LIFEPAK 20 LIFEPAK 20e - Stryker CorporationQUIK-COMBO® pacing/defibrillation/ECG elec trodes —...

SERVICE MANUAL

LIFEPAK® 20

LIFEPAK 20eDefibrillator/Monitor

©2002-2016 Physio-Control, Inc.

3202007-005

LIF Table of Contents

Back Index Next Page

C

Device Description

Modes of Operation

Preventive Maintenance

Battery Maintenance

EPAK 20/20e Defibrillator/Monitor

Title Page

lick a Topic

Preface Safety

Performance Inspection Procedures

Troubleshooting

Replacement Procedures

LIFEPAK 20/20e Specifications

P Back Index Next Page

LIF Section Contents

P maintain, test, troubleshoot, and repair the IFEPAK 20e defibrillator/monitor (device).20 Defibrillator/Monitor Operating PAK 20e Defibrillator/Monitor Operating by physicians, clinicians, and emergency tions provide step-by-step instructions, as intenance.t. Text that indicates the name of a button, ssage, or screen overlay appears in all utton and SETUP menu.

cs:

ernual

ations

(Continued on next page)

revious Page Table of Contents


reface This service manual describes how toLIFEPAK 20 defibrillator/monitor or LSeparate publications, the LIFEPAKInstructions (MIN 3200750) and LIFEInstructions (MIN 3205878), are usedcare providers. The operating instrucwell as operator-level testing and maNote: Hyperlinks appear in blue tex

menu, menu item, screen mecaps, for example, ANALYZE b

This section covers the following topi

TrademarksUsing Adobe Acrobat ReadNavigating Through the MaViewing the PIP ChecklistService Personnel Qualific



Pion



reface (continued) Contacting Physio-ControlResponsibility for InformatDevice TrackingService InformationWarranty InformationConfiguration InformationGlossaryAcronyms


LIF Preface

Tr

OMBO are registered trademarks of

hock Advisory System are trademarks of

demarks of Adobe Systems Incorporated.tered trademarks.

f Tektronix Incorporatedred trademarks of Masimo Corporation.

1-4

revious Page Table of Contents Section Contents


ademarks

LIFEPAK, FAST-PATCH, and QUIK-CPhysio-Control, Inc.CODE SUMMARY, REDI-PAK, and SPhysio-Control, Inc.Adobe and Acrobat are registered traFluke and Fluke Biomedical are regisTektronix is a registered trademark oMasimo, SET, and LNOP are registe© 2002–2016 Physio-Control, Inc.PN 3202007-005

Publication date: 03/2016


LIF Preface

U

AcRe

Acrobat Reader. The Adobe Reader can internet URL http://www.adobe.com/ssistance using the Adobe Reader ELP in the HELP menu.

Us left side of the screen. They enable you to e manual, similar to a table of contents. n, click the BOOKMARKS tab located to the

e desired topic. kmark topic indicates additional topics exist lick the plus sign to expand or collapse the

Us left of the screen to view miniature images through the pages and click an image to

1-5



sing Adobe Acrobat Reader

cessing Adobe ader Help

This service manual opens in Adobebe downloaded for free at the Adobeproducts/reader.html. For additional aprogram, access ACROBAT READER H

ing Bookmarks Bookmarks appear in a column on theeasily navigate to main sections of thTo view or hide the bookmarks columfar left of the screen. To jump to a bookmark topic, click thNote: A plus sign to the left of a boo

under that bookmark level. Cbookmarks.

ing Page View Click the PAGES tab located to the farof each page in the document. Scrolljump quickly to that page.

http://www.adobe.com/products/reader.html

http://www.adobe.com/products/reader.html


LIF Preface

N

link to jump to that topic. Click each page to return to your previous inting finger when positioned over a link. h page also provides helpful links. The

jump to the main table of contents for the

mp to the table of contents for the section

dex.

teps in a document, returning to each page

next page of the manual.

to the previous page of the manual.vigation bar above the main bar that ics.

Back

1-6



avigating Through the Manual

Blue text indicates a hyperlink. Click ain the navigation bar at the bottom oflocation. The pointer changes to a poA navigation bar at the bottom of eacnavigation bar includes:■ Click to

manual.

■ Click to juyou are currently viewing.

■ Click to jump to the in

■ Click to retrace your sin the reverse order visited.

■ Click to jump to the

■ Click to jump Some pages include an additional naprovides access to closely related top

Table of Contents

Section Contents

Index

Back

Next Page

Previous Page


LIF Preface

V

ance Inspection Procedure Checklist is

ing the file in Acrobat Reader.

1-7



iewing the PIP Checklist

The LIFEPAK 20/20e device Performincluded on this CD-ROM.You can view this document by open


LIF Preface

S

qualified and thoroughly familiar with the e familiar with and be able to read and must meet at least one of the following

th an emphasis in biomedical electronicswith an emphasis in biomedical electronics experience

1-8



ervice Personnel Qualifications

Service technicians must be properlyoperation of the device. They must bunderstand the service manual. Theyrequirements (or the equivalent):■ Associate of Applied Science, wi■ Certificate of Technical Training, ■ Equivalent biomedical electronics


LIF Preface

C

lands B.V.

1-9



ontacting Physio-Control

Physio-Control, Inc.11811 Willows Road NortheastRedmond, WA 98052-2003 USATelephone: 1.425.867.4000Toll Free (USA only): 1.800.442.1142Fax: 1.425.867.4121Internet: www.physio-control.com

Physio-Control Operations NetherGaljoenweg 686222 NV MaastrichtThe Netherlands

Physio-Control Australia Pty LtdSuite 4.0115 Orion RoadLane CoveNSW 2066Australia

http://www.physio-control.com


LIF Preface

R

thods required to maintain, test, and repair peration of the device. Qualified service ate operating instructions and this service anding of the use and maintenance of the

rs to ensure that the appropriate person(s) o the information in this service manual, used throughout the manual.

1-10



esponsibility for Information

This service manual describes the methe device. It does not address the opersonnel must consult the approprimanual to obtain a complete understdevice.It is the responsibility of our customewithin their organization has access tincluding any warnings and cautions


LIF Preface

D

ion requires defibrillator manufacturers and ir devices. If your device has been sold,

stroyed, or if it was not obtained directly e device-tracking coordinator at ting instructions for more information

1-11



evice Tracking

Device Tracking:

The U.S. Food and Drug Administratdistributors to track the location of thedonated, lost, stolen, exported, or defrom Physio-Control, please notify th1.800.426.4448. Refer to your operaconcerning device tracking.

!USA


LIF Preface

S

ny assembly in the device, the service information provided in the Preventive

ld inspect any device that has been ify that the device is operating within erformance Inspection Procedure (PIP), re acceptable.vice are limited to those items accessible at s and adjustments must be made by

ents at the subassembly level simplify help ensure correct device operation and mblies that require software may require ce representative. maintenance for your device, contact your In the USA, call Physio-Control Technical he USA, contact your local Physio-Control

1-12



ervice Information

Before attempting to clean or repair atechnician should be familiar with theMaintenance section of this manual.A qualified service technician shoudropped, damaged, or abused to verperformance standards listed in the Pand that the leakage current values aReplacement procedures for the dethe subassembly level. Replacementqualified service personnel. Replacemrepair and servicing procedures and calibration. Printed circuit board asseinstallation by a Physio-Control ServiTo obtain Physio-Control service andlocal service or sales representative.Support at 1.800.442.1142. Outside trepresentative.


LIF Preface

W

ided with the LIFEPAK 20 defibrillator/

MAg

purchase of this device does not convey the device with replacement parts that

this device, fall within the scope of one or vice.

1-13



arranty Information

Refer to the warranty statement provmonitor.

asimo® Use reement

No Implied License — Possession orany express or implied license to usewould, alone, or in combination with more of the patents relating to this de


LIF Preface

Bseful life.

e should be recycled according to national tions on disposing of this product or its sio-Control.com/recyclingbe clean and contaminant-free prior to

s – After using disposable electrodes, es for recycling.ce uses rechargeable Lithium-ion batteries. ctions provided in this service manual for as described. recycled according to national and local

1-14



attery Recycling Information Recycle the device at the end of its u

■ Recycling assistance – The devicand local regulations. For instrucaccessories, see http://www.Phy

■ Preparation – The device should being recycled.

■ Recycling of disposable electrodefollow your local clinical procedur

■ Recycling of batteries – The deviFollow local guidelines and instrudiscarding and recycling batteries

■ Packaging – packaging should beregulations.

http://www.physio-control.com/recycling/?terms=recycle


LIF Preface

C

evices and options through the following

itor basic device with ECG

1-15



onfiguration Information

This service manual covers existing drevisions:■ LIFEPAK 20/20e defibrillator/mon■ Pacing option■ SpO2 option


LIF Preface

G

used throughout this service manual. AED) — The device uses an ECG analysis ise the device operator if it detects a m. For more information, refer to the Shock perating instructions.k waveform generated by the device. The ed by a positive current phase, followed by r duration and decreased magnitude. The biphasic truncated exponential (BTE).summary report that consists of a , and waveforms associated with certain

ement section in the operating instructions eport.


1-16



lossary

The following are definitions of terms■ Automated external defibrillator (

Shock Advisory System™ to advshockable or nonshockable rhythAdvisory System section in the o

■ Biphasic technology — The shocbiphasic waveform is characteriza reverse current phase of shortewaveform pulse characteristic is

■ CODE SUMMARY™ report — A preamble, an event/vital signs logevents. Refer to the Data Managfor a sample CODE SUMMARY r


LIF Preface

Gystem (CPSS) — A feature that monitors LES for a potentially shockable rhythm.

DE indicator is on or the VF/VT ALARM is S button (manual mode). The CPSS hock Advisory System. For more visory System section in the operating

llation/ECG electrodes — An electrode fibrillation therapy to the patient.ion/ECG electrodes — An electrode system defibrillation therapy to the patient.

A combination lead tester/patient cardiac s designed for use in training clinical device.


1-17



lossary (continued) ■ Continuous patient surveillance s

the patient ECG in LEADS or PADDCPSS is active when the AED MOselected after pressing the ALARMoperates in conjunction with the Sinformation, refer to the Shock Adinstructions.

■ FAST-PATCH® disposable defibrisystem that allows delivery of de

■ QUIK-COMBO® pacing/defibrillatthat allows delivery of pacing and

■ QUIK-COMBO patient simulator —rhythm simulator. The simulator ipersonnel in the operation of the


LIF Preface

G— A variant of the QUIK-COMBO pacing/tem. The system allows QUIK-COMBO e cable connection without removing the led pouch until needed.puterized ECG analysis system used to ore information, refer to the Shock

perating instructions.meter that checks the saturation of oxygen

o connect the test load to the patient

Agent — Software application that allows onfiguration and software updates. For System refer to internet: www.physio-

1-18



lossary (continued)

■ REDI-PAK™ preconnect system defibrillation/ECG electrodes syspacing/defibrillation/ECG electrodelectrodes from their air-tight sea

■ Shock Advisory System — A comdetect a shockable rhythm. For mAdvisory System section in the o

■ SpO2 — A noninvasive pulse oxiin arterial blood.

■ Test plug — An accessory used tconnector on the device.

■ LIFENET Asset, LIFENET Devicethe user to change device user cmore information about LIFENETcontrol.com




LIF Preface

Ad abbreviations used in this manual.

dvancement of Medical Instrumentationversionefibrillator

ciationtandards Institutexponential external body connection

direct cardiac connectionuscitationniturveillance system

or


1-19



cronymsThe following is a list of acronyms an

Term DescriptionAAMI Association for the AADC Analog-to-digital conAED Automated external dAh Ampere hourAHA American Heart AssoANSI American National SBTE Biphasic truncated eBF Electrically isolated, BPM Beats per minuteCF Electrically isolated, CPR Cardiopulmonary resCPU Central processing uCPSS Continuous patient sDMM Digital multimeterDSP Digital signal process


LIF Preface

A

ronous receiver/transmitter

ervicee

l Commission

Alert Program

anufacturer


1-20



cronyms (continued).Acronyms

Term DescriptionDUART Dual universal asynchECG ElectrocardiogramEMS Emergency medical sESD Electrostatic dischargESU Electrosurgical unitHR Heart rateIEC International ElectricaLCD Liquid crystal displayLED Light-emitting diodemmHg Millimeters of mercuryNHAAP National Heart AttackNSR Normal sinus rhythmOEM Original equipment mPC Personal computerPCB Printed circuit board


LIF Preface

A

on procedure

et computer

olatile random-access memory

rocedurerent

ia

1-21



cronyms (continued)

Term DescriptionPIP Performance inspectiPPM Pulses per minuteRISC Reduced instruction sRR Respiration rateRTC/NVRAM Real-time clock/non-vSSD Static-sensitive deviceTCP Test and calibration pVAC Volts, Alternating CurVF Ventricular fibrillationVT Ventricular tachycard



S fety conventions, terms, and symbols used e. This information is intended to alert recautions in the care, use, and handling of

tions



22afety This section describes the general sain this service manual or on the devicservice personnel to recommended pthis medical device.

TermsGeneral Warnings and CauSymbols


LIF Safety

Te

ervice manual or on the various ize yourself with their definitions and

ill result in serious personal injury or death.es that could result in serious personal

es that could result in device or property

st for more efficient or convenient device mation or explanation concerning the

2-2



rms

The following terms are used in this sconfigurations of the device. Familiarsignificance.Danger: Immediate hazards that wWarning: Hazards or unsafe practic

injury or death.Caution: Hazards or unsafe practic

damage.Note: Points of particular intere

operation; additional inforsubject under discussion.


LIF Safety

G

nd cautions. Keep these warnings and he device. More specific warnings and ice manual and the operating instructions.

s up to 360 J of electrical energy. Unless rating instructions, this electrical energy may ttempt to operate or service this device unless f all controls, indicators, connectors, and

rmed by properly trained individuals. This rges accessible inside the device at any time –

efully for discharging the A13 Energy Storage

any portion of this device in water or other device or accessories. If the device is ever ove the batteries and disconnect ac power until

interconnected to each other can be a source e that all equipment is interconnected safely


2-3



eneral Warnings and Cautions

The following are general warnings acautions in mind when working with tcautions appear throughout this serv

WARNINGShock hazard. The defibrillator deliverproperly used as described in the opecause serious injury or death. Do not athoroughly familiar with the function oaccessories.

Servicing of this device must be perfodevice may retain potentially lethal chaeven when off. Follow procedures carCapacitor.

Shock or fire hazard. Do not immerse fluids. Avoid spilling any fluids on theimmersed in water or other fluids, remthe device can be serviced.

Equipment or accessories improperly of ignition or cause a shock. Make sur


LIF Safety

G

trical shock, this equipment must only be tective earth.

or ECG/sync connector must be battery C power according to EN 60601-1.

ot service this device in the presence of en sources.

e directly above the patient. Place the device in tient should it fall from its shelf or other mount

ice may be damaged by mechanical or physical ropping. If the device has been abused,

ed service personnel.

2-4



eneral Warnings and Cautions (continued)

WARNINGShock hazard. To avoid the risk of elecconnected to a supply mains with pro

All equipment connected to the systempowered or electrically isolated from A

Possible fire or explosion hazard. Do nflammable gases, anesthetics, or oxyg

Patient hazard. Do not mount the devica location where it cannot harm the pa

CAUTIONPossible equipment damage. This devabuse such as immersion in water or dremove it from use and contact qualifi


LIF Safety

Sat may be used in this service manual or on nd accessories. Some symbols may not be ry country.

of type CF terminal

tected, type BF patient connection

connection

g instructions (symbol is black on white

g instructions

lt accompanying documents.

(symbol is black on yellow background)

ltage

rotective earth connection


2-5



ymbols The following list includes symbols thvarious configurations of the device arelevant to your device or used in eve

Defibrillation-pro

Defibrillation pro

Type BF patient

Consult operatinbackground)Consult operatin

Attention, consu

General warning

Warning, high vo

Safety ground. P


LIF Safety

S

nnector

l

l

ection to the ac mains)

nnection from the ac mains)


2-6



ymbols (continued)

Equipotential co

Positive termina

Negative termina

AC voltage

DC voltage

On (power: conn

Off (power: disco

Power on/off

Switch on

Switch off

[signal] Input


LIF Safety

S

t

or/data in

utton

ator shock

on screen


2-7



ymbols (continued)

[signal] Output

Sync in/ECG ou

System connect

HOME SCREEN b

Alarm off

Alarm on

Biphasic defibrill

Shock button

Shock count (x)

Joules

(x)

J


LIF Safety

S

n paddle

n paddle

rnal pacing

invasive pacing

arker


2-8



ymbols (continued)

Adult defibrillatio

Infant defibrillatio

Pace arrow, inte

Pace arrow, non

R-wave sense m

Event marker

Heart rate

Greater than

Less than


LIF Safety

S

nced

dicator

evice (SSD)

ity according to the European Medical 93/42/EECards Association certification for Canada tates

tion for Canada and the United States

ponent mark for Canada and the United

ity to ACA standards


2-9



ymbols (continued)

VF/VT alarm on

VF/VT alarm sile

Battery status in

Fuse

Static-sensitive d

Mark of conformDevice DirectiveCanadian Standand the United S

Intertek certifica

Recognized comStates

Mark of conform


LIF Safety

S

cable

kwise to unlock

te of manufacture)

used for placing orders

tem number

epresentative

wn: yyyy-mm-dd

ch code)


2-10



ymbols (continued)

Device to device

Turn countercloc

Manufacture (da

Serial number

Catalog number

Manufacturer’s i

Authorized EC r

Reorder number

Use by date sho

Single use only

Lot number (bat

YYYY

REF

LOT YYWW or YYMMDD


LIF Safety

Sf this product in the unsorted municipal

ispose of this product according to local www.physio-control.com/recycling for e proper disposal of this product.

a RoHS indicating the Environmentally riod (EFUP) denoting the number of years tance is likely to leak out into the

ripping water per IEC 60529

ces only

e, handle with care

ricts this device to sale by or on the order

er

2-11




ymbols (continued)

Do not dispose owaste stream. Dregulations. Seeinstructions on thSymbol for ChinFriendly Use Pebefore any subsenvironment.

Recycle this item

Protected from d

For USA audien

Fragile/breakabl

Federal law restof a physician

Protect from wat

!USA

http://www.physio-control.com/recycling

http://www.physio-control.com/recycling


LIF Safety

S

storage temperatures

atteries. Do not use NiMH batteries in this

2-12



ymbols (continued)

Recommended

This end up

Use only Li-ion bdevice.



DD

pics:

eatures, and Accessories



3evice escription

This section includes the following to

IntroductionPhysical Description and FOrdering Devices, SuppliesSystem Context DiagramsFunctional Description


LIF Device Description

In

Ab itor (device) is a complete, acute, cardiac-al and semiautomatic defibrillation e device enables the operator to deliver a the patient’s heart. Operators can plexity during normal operation.

En ated exponential (BTE) shock pulse for energy delivery is through self-adhesive G electrodes. When using these Es), internal circuitry continuously

electrodes and allows defibrillation only ttached to the patient. The user can select for energy delivery (for example, standard

3-2



troduction

out the Device The LIFEPAK 20/20e defibrillator/moncare response system with both manuoperation. When clinically indicated, thbrief, high-energy pulse of electricity topreconfigure the device to reduce com

ergy Delivery The device generates a biphasic truncdefibrillation. The standard method of QUIK-COMBO pacing/defibrillation/ECdisposable defibrillation electrodes (DDmeasures the impedance between thewhen the defibrillation electrodes are afrom a variety of optional accessories paddles or internal paddles).



In

MOp

off), the device enables the operator to e a charge sequence, and apply energy in hen the operator selects the VF/VT ALARM

s patient surveillance system (CPSS) able rhythm. A suspect rhythm alerts the

n message. The operator can then follow dministration of defibrillation therapy.

AE , the device uses the CPSS to monitor the A suspect rhythm alerts the operator with he operator may continue by pressing the ck Advisory System to analyze the ECG he operator can then follow locally ration of defibrillation therapy. For more visory System, refer to Appendix E in the

3-3



troduction (continued)

anual Mode eration

In manual mode (AED MODE indicatormanually select an energy level, initiateither direct or synchronized modes. Wfrom the ALARMS menu, the continuoumonitors the patient’s ECG for a shockoperator with a priority tone and screelocally established guidelines for the a

D Mode Operation In AED mode (AED MODE indicator on)patient’s ECG for a shockable rhythm.a priority tone and screen message. TANALYZE button, which allows the Shorhythm and make recommendations. Testablished guidelines for the administinformation about CPSS and Shock Adoperating instructions.


LI Device Description

InDF

:

D) defibrillation manual mode

y and ECG electrodes

es of operation

data at each event stamps for eventsarted events for printout

at onceximetry (SpO2) readoutte readout

sense markerstion/ventricular tachycardia and sounds a

d diagnostic functions.

3-4

Previous Page Table of Contents Section Contents

FEPAK 20/20e Defibrillator/Monitor


evice Primary unctions

The device has four primary functions■ Defibrillation

– Manual or semi-automatic (AE– Synchronized cardioversion in– Leads-off detection for therap

■ Noninvasive pacing– Demand and nondemand mod

■ Capture patient information– Stores both patient and device– Real-time clock provides time– Provides operator review of st

■ Patient signal monitoring– Displays up to two waveforms– Displays a continuous pulse o– Displays a continuous heart ra– Displays waveform pace and – Monitors for ventricular fibrilla

warning alarm– Prints continuous ECG data

Service features include calibration an



In

As ase assembly and optional extension ules/PCBs:

l components:

4. Therapy PCB5. User Interface PCB6. OEM modules

7. System connector panel module8. Internal ac to dc power supply9. Internal battery10. Internal cables

4. Internal paddles5. Standard paddles

3-5




semblies The device consists of a three-piece cmodule that enclose the following mod

and the following OEM and mechanica

and the following attachments:

1. System Control PCB2. Patient Parameter PCB 3. Power module

1. Display2. Speaker3. User controls and indicators4. Printer 5. SpO2 acquisition6. Patient connector panel

1. ECG 3- or 5-wire cables2. QUIK-COMBO cable3. SpO2 cable



In

Depe

s 1 device with battery backup.ent connection. Therapy, SpO2, and CO2

ent connection.

3-6

Ite ms 20–29




vice Classifications r IEC 60601-1

Defibrillator—Externally powered ClasApplied parts—ECG is a Type CF patiare Type BF patient connections.Internal electrodes are a Type CF pati

ms 1–6 Items 7–13 Items 14–19 Ite



P

LIFr

, indicators and connectors shown below, click items bar at the bottom of the page.

11 15 1612 1413

17

24

18192021

23

25

22

29

28

27 26


Items 20–29 Back to Illustration

3-7



hysical Description and Features

FEPAK 20/20e ont Panel

For information about the buttonsthe appropriate right arrow on the

123

4567

8 9 10

Items 7–13 Items 14–19



P ed)

LIFr(c


or liquid crystal display (LCD) screen displays waveforms, status messages, setup menus,

s to activate user-defined events. — Press to return to the home screen of the ture you are configuring. Pressing this button specific screen; instead, it returns to the ode or event you are configuring.

ol — Press to print the CODE SUMMARY

to start and stop the printer. the ac power (line power) is connected, the

dy.

3-8

Ite Items 20–29 Back to Illustration



hysical Description and Features (continu

FEPAK 20/20e ont Panel ontinued)

Number Description

1 Display screen — Coloperating messages, and so forth.

2 EVENT control — Pres3 HOME SCREEN control

particular option or feadoes not take you to ahome screen for the m

4 CODE SUMMARY contrcritical event record.

5 PRINT control — Press6 AC Mains LED - When

AC mains light is stea

ms 1–6 Items 14–19



P ed)

LIFr(c

— Illuminates when the device enters nto the Service Log (accessed through the er to Troubleshooting for information about

r — Connection port for the electrically cable.r — Connection port for the pulse oximeter. Infrared connection port provides wireless

ata management devices (this feature is not lease).— When active (SPEED DIAL LED is on), turn ake a selection from the menu or overlay ; press to confirm your selection.lluminates when the SPEED DIAL is active.ress to activate and silence alarms.


3-9

Ite Items 20–29 Back to Illustration





Number Description

7 Service indicator LEDservice error codes iSERVICE menu). Refthe error codes.

8 ECG cable connectoisolated ECG patient

9 SpO2 cable connecto10 IrDA port connector —

communications to davailable with this re

11 SPEED DIAL selector (either direction) to mshown on the screen

12 SPEED DIAL LED — I13 ALARMS control — P

ms 1–6 Items 7–13



P ed)

LIFr(c

ress to access the OPTIONS menu.ector — Connection port for the following:O electrodes (standard)

H electrodes (with optional cable)lectrodes (optional)ult and pediatric paddles (optional)les (optional)

ddle (optional) audio voice prompts and alert tones.

ess to temporarily slow the pacing rate. Press to adjust the pacing current.s to select a pacing rate.


3-10

Ite Back to Illustration





Number Description

14 OPTIONS control — P15 Therapy cable conn

– QUIK-COMB– FAST-PATC– REDI-PAK e– Standard ad– Internal padd– Posterior pa

16 Speaker — Provides17 PAUSE control — Pr18 CURRENT control —19 RATE control — Pres

ms 1–6 Items 7–13 Items 14–19



P

LIFr(c o activate the pacer function.

activate the synchronized mode.o discharge the device. to charge the device.

Press to select the energy levels in

n the device on and off. Illuminates when

hange the ECG size.change the ECG lead. to activate the Shock Advisory System.

— Illuminates when device is in AED

3-11



hysical Description and Features (continued)


Number Description

20 PACER control — Press t21 SYNC control — Press to22 SHOCK control — Press t23 CHARGE control — Press24 ENERGY SELECT control —

manual mode.25 ON control — Press to tur

the device is turned on.26 SIZE control — Press to c27 LEAD control — Press to 28 ANALYZE control — Press29 AED MODE indicator LED

mode.



P

LISi

Printer — Prints ECG waveforms, CODE SUMMARY reports, and related informationPrinter button — Opens printer door (for paper installation)

3-12




FEPAK 20/20e de Panel



P

LIBa

nnector — Connection port for ac (line) arning - Shock hazard on Page 2-4.

ector — Connection port for RS-232 ce. See Warning - Shock hazard on

onnector. See Warning - Shock hazard .tud

3-13




FEPAK 20/20e ck Panel

1 432

Number Description

1 AC power copower. See W

2 System connserial interfaPage 2-4.

3 ECG/Sync con Page 2-4

4 Grounding s



P

WBa

ts shown below. For additional information s, Supplies, and Training Tools in the he operating instructions.

QUIK-COMBO electrodes

3-lead ECG cable

OMBO therapy cable

(3-pack) ECG electrodes

pO2 sensor packot included with

Nellcor option)

LIF

LIF

Q

QUIK-COMBO test plug

LIF

S

3-14




hat Is Shipped with a sic Device

A basic device includes the componenabout components, refer to AccessorieMaintaining the Equipment section of t

QUIK-C

Operating instructions

(3) rolls 50 mm printer paper S

(N

In-Service DVD

AC power cord

EPAK 20 defibrillator/monitor

Operational DVD

Service Manual

Quick GuideEPAK 20 defibrillator/monitor

uick Reference Card

EPAK 20 defibrillator/monitor

ervicing CD- ROM



O s

Th tions, supplies, and accessories that are av

It MIN CAT.LB

3313180-004 26500-0035023313187-004 26500-003504804700-003 11240-0000133308666-000 21300-0080758036503205874-002 26500-0019603202149-001 26500-001050

Q 3006570-007 11110-0000403202674-002 11996-000017

3201673-000 11113-000002


3-15



rdering Devices, Supplies, and Accessorie

e following table (provided for reference) summarizes optional configuraailable. For ordering instructions, refer to Ordering Parts.

em DescriptionIFEPAK 20/20e defibrillator/monitorasic device Device with printer; includes:

■ LIFEPAK 20 operating instructions, English■ LIFEPAK 20e operating instructions, English■ 50-mm printer paper (package of 3)■ LIFEPAK 20e In-Service DVD Assembly■ Power cord■ LIFEPAK 20 Quick Guide, Clinical Training■ Accessory order form

UIK-COMBO ■ QUIK-COMBO therapy cables■ QUIK-COMBO electrodes with REDI-PAK™

preconnect system■ QUIK-COMBO test plug



O s (continued)

Yo template provided with the device. Place the uide to drill the holes for the screws that seNo lling the docking station.

It MIN CAT.S 3201655-003 11171-000007

3201655-001 11171-0000083201655-011 11171-0000173201655-010 11171-000016

E 3006218-02 11110-0000293006218-03 11100-000030800139-003 11100-000001

5 3200496-00 11110-0000663200496-01 11110-000067

S 3200936-013 11130-000037D 3201551-002 21330-000996

3-16



rdering Devices, Supplies, and Accessorie

u can install the docking station on any flat surface using the installation template where you want to install the docking station and use it as a g

cure the device.te: Ensure that the device has an adequate turning radius before insta

em DescriptionpO2 -option ■ LNOP® reusable adult finger sensor

■ LNOP SpO2 cable, 2.4 m (8 ft)■ LNCS reusable adult finger sensor■ LNCS SpO2 cable, 3.6 m (10 ft)

CG ■ 3-lead ECG cable (AHA)■ 3-lead ECG cable (IEC)■ ECG electrodes (package of 3)

-wire ECG -option ■ 5-wire ECG cable (AHA)■ 5-wire ECG cable (IEC)

tandard Paddles ■ Standard Paddles (Eng)ocking Station ■ Docking station and installation template



S

Fr how the device connects with external teries, and power devices.


IK-COMBO rapy cable IK-COMBO

lectrodes) Standard paddles

AP

EX

STE

RN

UM

3-17



ystem Context Diagrams

ont of Device The system context diagrams illustrateequipment, including accessories, bat

QUthe

(QUe

SpO2 cable

5-lead ECG cable

ECG electrodes pack

3-lead ECG cable

(3) rolls 50 mm printer paper



S

Ba

System connector

Grounding stud

3-18



ystem Context Diagrams (continued)

ck of Device

AC power cord

ECG/sync connector



F

In tor is a medical device capable of monitoring features. In addition to defibrillation, manual defibrillation, and pO2 and ECG monitoring. This device

ple, a hospital or therapy center) and is n additional internal battery for use as a

ntended to provide service personnel with sign. Its purpose is to assist qualified o the subassembly level. Troubleshooting e factory is not recommended, nor is it

to provide the detail necessary to support

pages as you review the descriptions that

3-19



unctional Description

troduction The LIFEPAK 20/20e defibrillator/monicombining a variety of therapeutic andautomatic defibrillation, semiautomaticnoninvasive pacing, the device offers Sshould be used indoors only (for exampowered by ac (line) power. There is abackup to ac power.The following functional description is ia basic understanding of the device deservice technicians in troubleshooting tbelow the subassembly level outside thwithin the scope of this service manualsuch repairs.Refer to the diagrams on the next two follow.



FSy w the descriptive text.

W01 Therapy

Connector

W02 Speaker

A04 Therapy PCB

A03 Power Module

A13 Capacitor

A14 Inductor

W11ECG Out/Sync InRS-232

7 ry

A09 AC Power Supply

A19 EMI Line Filter

B

S

I

CPU

Relay

Pacer

H-BridgePacer Supply

Cap Charger

Sonalert RS-232 DriversPower

Supplyr

Battery Charger

3-20



unctional Description (continued)

stem Block Diagram Click a link in the diagram below to vie

A01 System PCBA05 User Interface PCBA15

Keypad

A02 Patient Parameter PCB

W06 ECG Connector

A0Batte

W05 SpO2 Connector

A10SpO2 PCB

A06 OEM I/F PCB

A11 LCD

A08acklight

W04 peed Dial

W03rDA Port

A12Printer

DSPAudio Output

Paddles Pre-Amp

CPU

Data Bus

Companion Chip

Power Supply

DataBus

Power Supply

Power Switch

CPU

Data Bus

FPGA

Power Supply

Power Supply

Data Bus

CPUECG

Pre-AmpISO

Buffer

ISOP/S

UART

CPU

PoweMux



F

A0PC

es the central control for the device. A C) processor, along with a real-time clock al processing unit (CPU). A companion faces required within the device, including ication ports. The data bus provides high-1 System Control PCB and other PCBs

tem Control PCB are as follows:em Control PCB uses SW_VBatt A04 Therapy PCB to originate five power B as follows:

log ECG out, audio output circuitry, and

essor memory, companion chip and CPU

al signal processor processor chip

analog power for the paddles pre-amp


3-21




1 System Control B

The A01 System Control PCB providreduced instruction set computing (RISand digital memory, serve as the centrchip provides most of the discrete interthe RS-232 and IrDA external communspeed communication between the A0within the device. The major subsystems on the A01 Sys■ Power Supplies — The A01 Syst

(switched battery voltage) from thesupplies for use throughout the PC– ±5 V analog power for the ana

bus control– +3.3 V logic power for the proc

I/O– +2.5 V logic power for the digit– +2.0 V logic power for the CPU– Patient-isolated ±10 and ±5 V



F

A0PC

he paddles ECG pre-amplifier performs th filtering, and ECG sampling by means ADC) for the ECG signal received via the ADC are fed into the digital signal ring. Electrostatic discharge (ESD) and d for these signals as they pass through atient impedance is also measured using

The DSP completes ECG digital signal andwidth, acceptable for Shock Advisory ssing, and continuous ECG storage by ides the necessary audio processing for digital audio signals to the audio output

t circuitry provides digital-to-analog alog drive circuitry for the audio tones and fication are provided to drive the case of the device.

3-22




1 System Control B (continued)

■ Paddles ECG Pre-Amplifier — Tpatient-isolation, low-pass bandwidof an analog-to-digital conversion (therapy paddles. Results from the processor (DSP) for additional filtedefibrillation protection are providethe A04 Therapy PCB. Change in pa 57.1 kHz carrier.

■ Digital Signal Processor (DSP) —processing to a diagnostic quality bSystem, heart rate algorithm procethe CPU. In addition, the DSP provvoice prompts and tones, providingcircuitry.

■ Audio Output — The audio outpuconversion, filtering, and power anvoice prompts. Up to 2 W of ampliW02 Speaker located on the front



F

A0PC

ects ECG and SpO2 patient data, with the d provides preprocessed data to the algorithms, alarm control, operator rithms performed on the data before it is

nclude leads-off detection and internal sor (DSP) with digital memory makes up

performs these algorithms. System Control PCB through the data

tient Parameter PCB are as follows: nt Parameter PCB uses switched power power from the A07 Battery to originate e throughout the PCB as follows: CPU digital signal processor and memory A06 OEM Interface PCB drive the ECG pre-amp


3-23




2 Patient Parameter B

The A02 Patient Parameter PCB collexception of the paddles ECG data, ansystem controller for AED and R-wavedisplay and printout, and storage. Algosent to the A01 System Control PCB ipacer detection. A digital signal procesthe central processing unit (CPU) thatCommunication is provided to the A01bus. The major subsystems on the A02 Pa■ Power Supplies — The A02 Patie

from the A04 Therapy PCB with dcthree power supply voltages for us– +3.3 V logic power to drive the– +5 V analog power to drive the– ±5 V patient-isolated supply to



F

A0PC

re-amplifier performs the function of th filtering, and ECG sampling through

DC) for the ECG signal received through gnals are passed over the isolation barrier rocessing. The ECG pre-amplifier section G input.

A0 sponsible for selecting the best available s/PCBs in the system from the available built-in memory makes up the CPU. Therapy PCB through a serial interface. wer Module are as follows: er Module uses ORed_VBatt (battery the A09 AC Power Supply Module) to s for use throughout the PCB as follows:PU microcontroller and memory

the power pump for the RS-232 driver


3-24




2 Patient Parameter B (continued)

■ ECG Pre-Amplifier — The ECG ppatient-isolation, low-pass bandwidthe analog-to-digital conversion (Athe W06 ECG Connector. Digital siinto the DSP for additional signal psupports either 3-wire or 5-wire EC

3 Power Module The A03 Power module is primarily resource to power the rest of the modulepower sources. A microcontroller with Communication is provided to the A04The major subsystems on the A03 Po■ Power Supplies — The A03 Pow

voltage ORed with dc power from originate two power supply voltage– +5 V logic power to drive the C– + 3.3 V analog power to drive

circuits



F

A0(c

itches battery power in and out of VBatt, d load draw within the device. This circuit

CPU and provides the current voltage Power Supply Module to the CPU. The ac power to battery power if the voltage dly. Low voltage is detected by the broadcast to the other PCBs through the es.

fibrillator/monitor) — The battery charger ned specifically to support the A07 NiMH H batteries are not designed for trickle

pply Module keeps track of the amount of g from battery power. Charging is ents and periodically when the batteries ccur while the unit is powered on or while on need. The battery charger is designed lly in less than two hours.


3-25




3 Power Module ontinued)

■ Power Mux — The power mux swdepending on power availability anis under supervisory control of thefrom the A07 Battery and A09 AC circuit automatically switches fromfrom the ac power supply falls rapiA09 AC Power Supply Module anddevice internal communication bus

■ Battery Charger (LIFEPAK 20 deis a constant current charger desigBattery selected for the device. NiMcharging, so the A09 AC Power Sutime the device has been operatinperformed following high-use incidare not in high use. Charging can othe unit is powered off, depending to charge the internal battery, usua



F

A0(c

fibrillator/monitor) — The battery charger ge charger designed specifically to

y selected for the device. Li-ion batteries g, so the A09 AC Power Supply Module tate-of-charge and, when it drops below harging of the battery (provided the

° C). Charging can occur while the device is powered off, depending on need. The cally charge the internal battery in less powered off and AC power is applied.io tone generator located on the power evice is turned off while not connected to

nal A07 Battery). This ac loss alert alarm setup is provided to temporarily disable

ce for shipment.nal originates on the A01 System Control

signal levels to ±12 V prior to the system

3-26




3 Power Module ontinued)

■ Battery Charger (LIFEPAK 20e deis a constant current-constant voltasupport the A07 Lithium Ion Batterare not designed for trickle charginkeeps track of the Li-ion battery's s85%, the battery charger initiates ctemperature is between 0° and 50is powered on or while the device battery charger is designed to typithan four hours when the device is

■ Sonalert — The sonalert is an audmodule that warns the user if the dac power (which depletes the intercan be turned off. A shipping modethis feature when packing the devi

■ RS-232 Drivers — The RS-232 sigPCB. The RS-232 drivers shift theconnector output.



F

A0 cing and defibrillation therapy features. he A04 Therapy PCB and the remainder microprocessor and digital memory PU) that manages communication with

rapy PCB are as follows: apy PCB uses SW_VBatt (switched er Module to originate five power supply B as follows:PU microprocessor and memorycing and therapy drive circuitwer for the pacing and therapy circuitsower for the pacing and therapy circuitsower for the pacing and therapy circuits


3-27




4 Therapy PCB The A04 Therapy PCB controls the paThe primary communication between tof the device is through the data bus. Amake up the central processing unit (Cthe A01 System Control PCB.The major subsystems on the A04 The■ Power Supplies — The A04 Ther

battery voltage) from the A03 Powvoltages for use throughout the PC– +5 V logic power to drive the C– ±15 V analog power for the pa– Patient-isolated 5 V analog po– Patient-isolated 15 V analog p– Patient-isolated 30 V analog p



F

A0(c

is a control circuit that detects the ON r Interface PCB or a timer event from the r up the device. This portion of the ll times, with very low quiescent current detected, this circuit switches VBatt wer) provided by the A03 Power Module e. Low Battery (Battery Fail) is detected to other PCBs if battery voltage falls normal operation is no longer feasible.is a high-voltage, patient-isolated circuit citor to the correct voltage for biphasic trol is provided by the CPU, and capacitor U for feedback. The cap charger is imum charge rates and to automatically when low battery voltage is detected.r power supply is a patient-isolated circuit citor up to the correct voltage for pacing. d voltage regulation is maintained locally voltage is provided back to the CPU for cuitry.


3-28




4 Therapy PCB ontinued)

■ Power Switch — A power switch button selection from the A05 UseA01 System Control PCB to poweA04 Therapy PCB is powered at adraw. When a power-on request is(battery and/or ac converted dc poto the remaining PCBs in the devicand a discrete signal is broadcast rapidly or reaches the point where

■ Cap Charger — The cap charger that charges the A13 Energy Capadefibrillation (2 to 360 joules). Convoltage is provided back to the CPdesigned to nominally provide maxscale back to slower charge rates

■ Pacer Power Supply — The pacethat charges the A13 Energy CapaControl is provided by the CPU, anwithin the pacer supply. Capacitor control through the cap charger cir



F

A0(c

ient-isolated circuit that creates the combination of silicon controlled rectifiers ransistors (IGBT) are used to place a e across the patient load, followed defibrillation pulse. The defibrillation

y and W01 Therapy Connector assembly e outside of the device. lated circuit that creates the pacing e circuitry is used to support the pacer by ibrillation Capacitor. A current drive is nt provided to the patient during pacing. t isolation from the pacing and se. The relay is closed when the pacing closed until the pacing current is set back

3-29




4 Therapy PCB ontinued)

■ H-Bridge — The H-Bridge is a patbiphasic defibrillation waveform. A(SCR) and insulated gate bipolar tpositive-oriented defibrillation pulsimmediately by a negative-orientedpulse is delivered through the relato the external therapy cable on th

■ Pacer — The pacer is a patient-isowaveform. A portion of the H-Bridgproviding energy from the A13 Defused to control the amount of curre

■ Relay — The relay provides patiendefibrillation circuitry when not in ucurrent is set above zero and staysto zero.



F

A0 esponsible for the presentation of the d to the printer, and for receiving all user een the UI PCB and the remainder of the processor and digital memory make up with the A01 System Control PCB. The onnection between the A05 UI PCB and

PCB are as follows: CB uses SW_VBatt (switched battery B to originate four power supplies for use

A11 Liquid Crystal Display (LCD) and the

processor and memory-programmable gate array


3-30




5 User Interface PCB The A05 User Interface (UI) PCB is racquired data to the screen display aninput. The primary communication betwdevice is through the data bus. A RISCthe CPU that manages communicationW18 UI Flex Cable provides physical cthe A02 Patient Parameter PCB.The major subsystems on the A05 UI ■ Power Supplies — The A05 UI P

voltage) from the A04 Therapy PCthroughout the PCB as follows:– +3.3 V logic power to drive the

A12 Printer– +3.3 V logic power for the CPU– +2.5 V logic power for the field



F

A0(c

(FPGA) — The Field-Programmable Gate e between the CPU and all the user orks in conjunction with the CPU to A11 Display, the data and strobe signals try for the keypad LEDs. The FPGA d switch matrix and W4 Selector into e CPU. ary user input control for the device. It omes, which are located on the rear side er keypad cover that attaches to the front

through holes in the front case and he domes when pressed by the user. The PGA and sent to the CPU for processing. ze the ON switch. It passes the signal to

A0MCo

s power to and collects SpO2 data from tion is to provide patient isolation between evice design. In addition, it provides pO2 module.


3-31




5 User Interface PCB ontinued)

■ Field-Programmable Gate ArrayArray (FPGA) provides the interfacinterface peripherals. The FPGA wprovide the 1/4 VGA signals to theto the A12 Printer, and drive circuiconverts the inputs from the keypadigital words that can be read by th

■ Keypad — The keypad is the primconsists of two parts, the keypad dof the A05 UI PCB, and the elastomcase. The keypad domes protrudeenable the key covers to activate tkey presses are decoded by the FThe A05 UI PCB does not recognithe A04 Therapy PCB.

6 OEM and echanical mponents PCB

The A06 OEM Interface PCB providethe A10 SpO2 Module. Its primary functhe SpO2 module and the rest of the dphysical mounting provisions for the S



F

A0MCo(c

M PCB are as follows: Interface PCB uses power from the vide the 5 V power for the A10 SpO2

RT and ISO buffers provide patient received from the A10 SpO2 Module and rameter PCB.

A0 r, the A07 Battery is a minimum 2.7 Ah , NiMH battery that is used as an internal

is not available. This technology was er-storage ratio and low maintenance rt, non-trickle, constant current charger ule when the device is connected to ac

aces directly with the A03 Power Module. tery well section of the bottom case. A open the battery door, located on the

/monitor.


3-32




6 OEM and echanical mponents PCB

ontinued)

The major subsystems on the A06 OE■ Power supplies — The A06 OEM

A02 Patient Parameter PCB to proModule.

■ UART and ISO buffers — The UAisolation for the serial data signalsroutes them to the A02 Patient Pa

7 Battery On the LIFEPAK 20 defibrillator/monito(2.560 Ah per IEC 61951-2:2011), 12 Vbackup power source when ac power selected due to its light-weight-to-powfeatures. NiMH batteries require a smathat is provided by the A03 Power Modpower. The battery wire harness interfThe battery is contained within the batsmall-bladed screwdriver is required tobottom of the LIFEPAK 20 defibrillator


LI Device Description

F

A0(c

itor, the Li-ion battery technology was H, but they are even lighter in weight.

rrent-constant voltage charger that is hen the device is connected to ac power.

A0PC

power to the internal fluorescent backlight _VBatt is provided to the A08 Backlight

ce PCB. The output of the inverter is er to the internal A11 Active Display er for the LED A11 Display has an output current of 24 mA dc

A0M

is a 60-Watt OEM power supply, designed erting 120/240 Vac (60/50 Hz) input signals ply provides power to the A03 Power

in the device. The 12 Vdc output from the ed into the SW_VBatt (switched battery y PCB. The A03 Power Module sits above ly into the ac power supply’s power le and the ac power supply are held ssembly bracket.

3-33




7 Battery ontinued)

On the LIFEPAK 20e defibrillator/monselected for the same reasons as NiMLi-ion batteries require a constant cuprovided by the A03 Power Module w

8 Backlight Inverter B

The A08 Backlight Inverter providesin the A11 Active Display. Filtered SWInverter through the A05 User Interfa1000 to 1500 RMS, open-circuit powbacklight. The 3308907 backlight drivaverage output voltage of 22Vdc and

9 AC Power Supply odule

The A09 AC Power Supply Moduleto meet IEC 60601-1 standards, convto nominal 12 Vdc. The ac power supModule for routing to the other PCBsac power supply is directly diode ORvoltage) to power on the A04 Therapthe ac power supply and plugs directconnector. Both the A03 Power Modumechanically in place by the power a



F

A1 simo MS-5, MS-11 or MS-2011 oximetry erforms all functions related to oxygen sor drive. Measurement results are

Interface PCB to the A02 Patient is combined with the patient ECG data CB for display processing and storage. he A06 OEM Interface PCB.

A1Le

.5 cm (5.7-inch) (measured diagonally) wide by 240 high pixel array. The display ainst the front case by a sheet metal display features full-color, high-lity, and is fully visible in bright-light ns). The A11 Active Display also contains -light situations. The updated A11 LED 08 backlight driver module 3308907.

A1 stepper motor-driven recorder. The printer m the A05 User Interface PCB, converts rive signals to perform the “muscle” part

ignals derived from the paper supply PCB.

3-34




0 SpO2 Module The A10 SpO2 Module can be the Mamodule. This patented OEM module psaturation measurement, including senpassed serially through the A06 OEM Parameter PCB where the SpO2 data and sent to the A01 System Control PThe SpO2 module mounts directly to t

1 Active Display/ns

The A11 Active Display measures 14and uses 1/4 VGA protocol with a 320has a protective lens, held in place agbracket, and an elastomeric seal. Thisbrightness, wide-viewing-angle capabisituations (up to direct sunlight operatioan internal backlight for visibility in lowdisplay 3309555 requires the use of A

2 Printer Module The A12 Printer Module is a 50 mm, receives serial data and commands frothe print data, and controls the motor-dof printing. The printer returns status ssensor and printer door to the A05 UI



F

A1 llized film capacitor used for energy nergy for both pacing and defibrillation e energy capacitor is calculated during The nominal value is 196 F. The energy device is turned off. Energy is provided to efibrillation therapy through the A14 r mounts above the A04 Power PCB by om the energy capacitor connect directly

A1 s an internal dump load to dissipate r. Energy is removed (dumped) from the is turned off and, during operation, when extended period of time. The inal 5 ohm load in the energy delivery stack bracket. Wires from the

y to connectors on the A04 Therapy PCB.

3-35




3 Energy Capacitor The A13 Energy Capacitor is a metastorage. The energy capacitor stores etherapies. The actual capacitance of ththe defibrillation calibration procedure.on the capacitor is removed when the the A04 Therapy PCB for pacing and dInductor Resistor. The energy capacitomeans of a capacitor support. Wires frto the A04 Therapy PCB.

4 Inductive Resistor The A14 Inductive Resistor is used aenergy from the A13 Energy CapacitoA13 Energy Capacitor when the deviceenergy remains on the capacitor for anA14 Inductive Resistor provides a nompath. The inductor mounts to the boardA14 Inductive Resistor connect directl



F

A1 the common device controls (those not umber of keys on this keypad varies, a specific device.

A1Fi

des input current overload and tection for the device. The filter is a potted nts (inductors and capacitors), with in-line . The A19 AC Input Power Filter is nts in IEC 60601-1.

WCo

bly provides a patient connection port or pacing therapeutic energies. The e attachment of all available electrode pacing/defibrillation/ECG electrodes, pediatric paddles), and internal paddles py Connector mounts directly to the s directly into the A04 Therapy PCB at otrudes through a hole in the front case to various external cable options.

g LIFEPAK 12 defibrillator/monitor l adult paddles with posterior

3-36




5 Elastomer Keypad The A15 Elastomer Keypad displaysavailable using the SPEED DIAL). The ndepending on the features installed in

9 AC Input Power lter

The A19 AC Input Power Filter provielectromagnetic interference (EMI) promodule containing passive filter elemefuses in both the line and neutral leadsdesigned to meet the safety requireme

01 Therapy nnector Assembly

The W01 Therapy Connector Assemused for delivery of either defibrillationstandard and premium models allow thaccessories, including QUIK-COMBO external standard paddles (with built-inwith discharge control. The W01 Therabottom case and the wire harness plugJ13 and J14. The therapy connector prprovide user access for connecting theNote: The device supports all existin

accessories (including externaattachments).



F

W to deliver device tones and voice prompts, M W02 Speaker is a small, compact, low-

one-watt output with a frequency ut to the speaker is from the audio power B. The speaker is mounted directly on

rness plugs into the W25 Speaker

W(Ir

rovide high-speed wireless devices. The OEM W03 IrDA port ions with asynchronous serial rates up to ted directly on the bottom case and the System Control PCB at J08. An infrared se directly in front of the IrDA port. The ed so that direct communications can ceiver held by an operator or placed on a

3-37




02 Speaker Assembly The W02 Speaker Assembly is used including warnings and alarms. The OEprofile speaker capable of producing aresponse from 300 to 7000 Hz. The inpamplifier in the A01 System Control PCthe front case and the speaker wire haHarness Extension Cable.

03 Infrared Data DA) Assembly

The W03 IrDA Assembly is used to pcommunications to data management supports IrDA version 1.1 communicat4 Mbits/second. The IrDA port is mounflex circuit connects directly to the A01lens is molded into the device front caIrDA port and front case lens are aligneasily be made with a portable data retable.



F

WAs

otary data entry device mounted on the ront case. It is used to control menu s that are not supported directly by hard cts rotation (in either a clockwise or es (clicks), and then passes this 32 for user-input decoding.

W connecting point for the external SpO2 d on the bottom case of the device, and A10 SpO2 Module.

W connection point for the standard 3-lead or onnector is mounted on the bottom case rness connects directly with the A05

ible with the 10-wire patient ECG cable, as a 5-wire cable.

WDi

rovides a capacitor discharge point by t pin 5 of J02.

3-38




04 Speed Dial sembly

The W04 Speed Dial Assembly is a rLIFEPAK 20/20e defibrillator/monitor faccess and selection for user functionkeys on the keypad. The selector detecounterclockwise direction) and pressinformation on to the A05 UI PCB at J

05 SpO2 Assembly The W05 SpO2 Assembly provides acable. The SpO2 connector is mountethe flex circuit connects directly to the

06 ECG Connector The W06 ECG Connector provides a 5-wire patient ECG cables. The ECG cof the device, and the attached wire haPatient Parameters PCB at J23. Note: The ECG connector is compat

but the device will only operate

07 Capacitor scharge Cable

The W07 Capacitor Discharge Cable pconnecting to the A04 Therapy PCB a



F

W r, the W08 Battery Cable connects the The cable is hardwired to the A03 Power the A07 Battery at J85.tor, the W08 Battery Cable connects the odule at J50.

WTh

PCB Cables connect the A03 Power is a replaceable cable that connects to e A03 Power Module at J41. r, W10 is hardwired to the A03 Power py PCB at J17.

tor, W10 connects to the A04 Therapy ule at J51.

WCa

onnect the ECG sync connector and the odule at J47.

W grounding path for the Speed Dial.

3-39




08 Battery Cable On the LIFEPAK 20 defibrillator/monitoA07 Battery to the A03 Power Module.Module and the other end connects toOn the LIFEPAK 20e defibrillator/moniA07 Battery at J85 to the A03 Power M

09/W10 Power to erapy PCB Cables

The W09 and W10 Power to Therapy Module to the A04 Therapy PCB. W09the A04 Therapy PCB at J16 and to thOn the LIFEPAK 20 defibrillator/monitoModule and connects to the A04 TheraOn the LIFEPAK 20e defibrillator/moniPCB at J17 and to the A03 Power Mod

11 ECG Sync/System bles

The W11 ECG Sync/System Cables csystem connector to the A03 Power M

12 Grounding Cable The W12 Grounding Cable provides a



F

W e A09 AC Power Supply Module at J02 d connection) for the LIFEPAK 20 LIFEPAK 20e defibrillator/monitor.

W he A05 UI PCB at J34 with the A03 Power

WCa

cts the A11 LCD Display PCB at CN1 with

WCa

der connects the A11 LCD Display PCB at at CN2.

WCa

nects the A08 Backlight Inverter PCB at

W 02 Patient Parameters PCB at J21 and

3-40




13 AC Power Cable The W13 AC Power Cable connects thwith the A03 Power Module (hard-wiredefibrillator/monitor, and at J49 for the

14 Printer Flex Cable The W14 Printer Flex Cable connects tModule at J45 and the A12 Printer.

15 LCD to UI PCB ble

The W15 LCD to UI PCB Cable connethe A05 UI PCB at J36.

16 Display Jumper ble Extender

The W16 Display Jumper Cable ExtenP77 to the A08 Backlight Inverter PCB

17 Backlight Inverter ble

The W17 Backlight Inverter Cable conP74 to the A05 UI PCB at J37.

18 UI Flex Cable The W18 UI Flex Cable connects the AJ22 to the A05 UI PCB at J31.



F

WCa

les provide grounding paths for various

WEx

Cable connects the W02 Speaker 5.

3-41




19 – W24 Grounding bles

The W19 through W24 Grounding Cabdevice components.

25 Speaker Harness tension Cable

The W25 Speaker Harness ExtensionAssembly to the A01 System PCB at J



MO

ates in one of five modes. Choose from the particular operating mode.

ation



55odes of peration

When the device is turned on, it operfollowing links to learn more about a

Manual ModeAED ModeSetup ModeSaving the Setup ConfigurService ModeInservice Mode


LIF Modes of Operation

M

Tuin

rmine when to deliver a shock. anual mode (the default is AED mode):

ct MANUAL MODE.UAL MODE submenu.

able power-on options.

and then reset to AED mode by pressing tional manual mode reprompts or wer has been cycled.

scriptionanual mode; direct access between AED odes.

ED mode; direct access between AED odes.

ED mode; confirmation required to enter .ED mode; passcode required to enter .


4-2



anual Mode

rning On the Device Manual Mode

Manual mode enables the user to deteTo configure the device to turn on in m1. Display the SETUP menu and sele2. Select MANUAL ACCESS in the MAN

3. Select the DIRECT option. The following table shows all the avail

If the device is placed in manual modethe ANALYZE button, there are no addipasscode requests until the device po

Mode/Response Response DeManual/Direct Turns on in m

and manual mAED/Direct Turns on in A

and manual mAED/Confirmed Turns on in A

manual modeAED/Passcode Turns on in A

manual mode



M

Stfro

device is turned on, the device is in AED

ssing the MANUAL button on the lower left

s:

YZE button or cycle the device power.nual mode does not restart AED mode

4-3



anual Mode (continued)

arting Manual Mode m AED Mode

If the AED MODE LED is on when the Mode. To enter manual mode:■ Open the door (if installed) by pre

corner of the door.-OR-

■ Press one of the following button– ENERGY SELECT– CHARGE– PACER– LEAD

To restart AED mode, press the ANAL

Note: Closing the door when in maoperation.



A

device automatically evaluates the patient ded and prompts the user to press the

rn on in manual mode, if desired. the SETUP menu and select AED MODE. otocol, voice prompts, ECG display, CPR cription of the options available, refer to the operating instructions.

D mode, opening the door on the device s the device in manual mode. Closing the de operation. To restart AED mode, press

power.

4-4



ED Mode

In AED mode (the default setting), therhythm to determine if a shock is neeSHOCK button to deliver a shock.The device can be reconfigured to tuTo set options for AED mode, displayAED mode options include energy prtime, and others. For a complete desDefining Setup Options section in theNote: If configured to turn on in AE

turns off AED mode and placedoor does not restart AED moANALYZE or cycle the device



S

In are configured in the SETUP menu. Options e operating characteristics, alarm setup,

is also a factory-reset option that resets the except the maintenance interval, which is complete, turn off the device to save the ce is turned on, the operating defaults last

ptions, refer to the Defining Setup Options


4-5



etup Mode

troduction The operating defaults for the device include manual mode and AED modtime-of-day clock, and others. There device to the factory default settings,remains unchanged. After the setup configuration. The next time the deviselected will be active.For a complete description of setup osection in the operating instructions.



S

DiM EVENT buttons, and then press the ON

DE overlay appears, release the buttons. indicating that the SPEED DIAL is active. SPEED DIAL to select a number and then er is selected, it changes to an asterisk for t digit in line highlights.de (0000) or the reserved technician

sed in place of other passcodes to gain E menus.code, press the SPEED DIAL. The SETUP CORRECT-TRY AGAIN message appears if

.ice OFF.


4-6



etup Mode (continued)

splaying the Setup enu

To display the SETUP menu:1. Press and hold the OPTIONS and

button. When the ENTER PASSCOThe SPEED DIAL LED illuminates,

2. To enter the passcode, rotate thepress the SPEED DIAL. As a numbpasscode protection, and the nexNote: The factory default passcopasscode (5433 or LIFE) can be uaccess to the SETUP and SERVIC

3. When you have entered the passmenu appears. The PASSCODE INan incorrect passcode is entered

To exit the SETUP menu, turn the dev



S

Se menu options.ptions section in the operating instructions ll options.

evice options

ode defaults

e defaults

faults

g defaults

ppear on the event overlay

faults

faults

time defaults

s to factory configuration settings


4-7




tup Menu Options The following table defines the SETUP

Note: Refer to the Defining Setup Ofor complete descriptions of a

Option Description

GENERAL Set up general dMANUAL MODE Set up manual mAED MODE Set up AED modPACING Set up pacing deMONITORING Set up monitorinEVENTS Set up items to aALARMS Set up alarms dePRINTER Set up printer deCLOCK Set up date and RESET DEFAULTS Reset all default



S

Se(c

SaCo

guration that cannot be disturbed, there p during repair procedures. System account, then use the LIFENET e setup configurations.sfer cable can be used to transfer the vice. After service is complete, transfer al device.

urrent configuration settings.

iguration to another device.

setup mode and archives mode.

CE menu.


4-8




tup Menu Options ontinued)

ving the Setup nfiguration

If the device owner uses a setup confiare choices available to preserve setu■ If the device owner has a LIFENET

Device Agent application to manag■ The LIFEPAK 20 configuration tran

setup configuration to another dethe configuration back to the origin

Option Description

PRINT DEFAULTS Print a report of cSEND CONFIG Send device confSET PASSCODE Set passcodes forSERVICE Display the SERVI



S

SaCo(c

nfiguration is to use SETUP menu to print service is complete, you can verify the e configuration. ansferring it to another device requires that software version. Otherwise, unexpected nfiguration is restored to the repaired

Cr SCODES in the SETUP menu. the SET PASSCODES submenu. .

enter setup mode.e access protocol for archives mode:(default) 3. Delete Only

4. Archive/Deleteenter archives mode.delete records in archives mode.


4-9




ving the Setup nfiguration

ontinued)

■ Another way to save the setup cothe setup configuration. When setup and then manually reset th

Note: Saving the configuration by trboth devices have the same results can occur when the codevice.

eating a Passcode To create a passcode, select SET PAS

Select one of the following options in

Option DescriptionSETUP MODE Set passcode to ARCHIVES ACCESS Select a passcod

1. No Passcode 2. Archives Only

ARCHIVES MODE Set passcode to DELETE RECORDS Set passcode to



S

Cr ce to any of the following protocols (refer to

ives mode and allow records to be deleted.rchives mode, but allow records to be

ves mode, but require a password to delete

rchives mode and delete records setup e to access the SETUP menu. The ENTER

ith the first digit highlighted. Rotate the

code to enter archives mode. The ENTER the first digit highlighted. Rotate the SPEED

scode to delete records in archives mode. pears with the first digit highlighted. Rotate

4-10




eating a Passcode ■ ARCHIVES ACCESS – Set the devithe table above):1. Allow unlimited access to arch2. Require a password to enter a

deleted.3. Allow unlimited access to archi

records.4. Require a password to enter a

MODE – Create a new passcodPASSCODE overlay appears wSPEED DIAL to select digits.

■ ARCHIVES MODE – Create a passPASSCODE overlay appears with DIAL to select digits.

■ DELETE RECORDS – Create a pasThe ENTER PASSCODE overlay apthe SPEED DIAL to select digits.



S

In ualified service technicians to:

ure must be performed from start to finish

on

rillation rationad Test Test

■ Printer Test■ Audio Test

e Log Statusce Log Statuse Data

■ Counters Status■ Clear Memory

valterval


4-11



ervice Mode

troduction The service mode functions enable q

* The performance inspection procedin the order presented.

Function Descripti

*Perform device calibration routines

■ DefibCalib

*Perform device tests ■ Keyp■ Pixels

View the device status registers

■ Devic■ Servi■ Devic

Set the service mode passcodeSet the maintenance prompt interReset the maintenance prompt in



S

DiM

enu. (0000 or 5433). ss the SPEED DIAL. The SERVICE menu e is entered, the PASSCODE INCORRECT -

Se

evice OFF.

tor calibration procedure.

nce inspection procedure.

tatus.

ode access passcode.

erform preventative maintenance.

ETUP menu.


4-12



ervice Mode (continued)

splaying the Service enu

To display the SERVICE menu:1. Display the SETUP menu.2. Select SERVICE from the SETUP m3. Enter the service mode passcode4. After you enter the passcode, pre

appears. (If an incorrect passcodTRY AGAIN message appears.)

rvice Menu Options The SERVICE menu options include:

To exit the SERVICE menu, turn the d

Option Description

Defib Cal Perform defibrilla

Tests Follow performa

Status Display device s

Set Passcode Set the service m

Maint Prompt Prompt user to p

Setup Return to main S



S

SeM VICE menu. The SERVICE/SET PASSCODE

SPEED DIAL to select a number and then

SERVICE menu appears.


4-13




tting the Service ode Passcode

To set a service mode passcode:1. Select SET PASSCODE in the SER

overlay appears.2. Enter a passcode by rotating the

pressing the SPEED DIAL. 3. When the last digit is entered, the



S

SePr

can be set to display a screen message ance prompt interval date has passed. The appears on the screen for the first d on. The device maintenance interval can

onths, or 12 months; the factory default is ice technician. e interval:

ICE/MAINT PROMPT submenu appears for scheduled maintenance (if set).ices are: OFF, 3 MONTHS, 6 MONTHS, and


4-14




tting a Maintenance ompt Interval

The LIFEPAK 20 defibrillator/monitorthat alerts the user when the maintenscreen message MAINTENANCE DUE 10 minutes after the device is powerebe turned off or set to 3 months, 6 mOFF, but it can be activated by a servTo change the scheduled maintenanc1. Display the SERVICE menu.2. Select MAINT PROMPT. The SERV

showing the current prompt date 3. Select INTERVAL. The interval cho

12 MONTHS.4. Select the desired interval.5. Turn the device OFF.



S

ReM

nce, reset the maintenance prompt counter age and begin the count for the next

intenance prompt:

CE/MAINT PROMPT menu appears, showing uled maintenance.

revised to the next scheduled maintenance

4-15




setting the aintenance Prompt

After completing scheduled maintenato clear the MAINTENANCE DUE messscheduled maintenance.To turn off or reset the scheduled ma1. Display the SERVICE menu.2. Select MAINT PROMPT. The SERVI

the current prompt date for sched3. Select RESET. The prompt date is

date.4. Turn the device OFF.



In

In ctice or demonstrate the monitoring include:e, and volume, and moving ECG waveform

able in the Inservice mode.

EnM e. Inservice mode cannot be entered if

.d EVENT buttons, turn the device ON. INSERVICE overlay appears.e OFF.

4-16



service Mode

troduction Inservice mode enables users to prafunctions of the device. The functions■ Selecting ECG lead selection, siz

with heart rate■ SpO2 ■ Alarms■ EventsNote: No therapy features are avail

tering Inservice ode

To enter Inservice mode:1. Remove all cables from the devic

cables are attached to the device2. While holding down the HOME an

Release these buttons when the To exit Inservice mode, turn the devic

Previous Page Table of Contents Back Index Next Page

LIFEPAK 20/20e Defibrillator/Monitor Section Contents

Performance Inspection Procedures

The Performance Inspection Procedures (PIP), document reference number 3201896, are a set of manual test procedures used for an operational closed-case evaluation of the LIFEPAK 20/20e defibrillator/monitor (device).The PIP describes the test procedures you will perform to determine if the device is operating within the required specifications. Investigate and correct any malfunctions or out-of-tolerance conditions detected during the PIP.The PIP is comprised of safety and performance tests recommended by AHA/ASHE (American Hospital Association/American Society for Hospital Engineering) Maintenance Management for Medical Equipment and International Electrotechnical Commission (IEC) Technical Report 1288-2, Maintenance of Cardiac Defibrillators-Monitors. Perform the PIP as part of a regularly scheduled preventive maintenance routine. Perform the PIP after any repair, replacement, or calibration procedure. Use the PIP Checklist to record test results. Refer to the Operator Checklist for additional items.



Tr code usage, interpretation, and corrective leshooting chart for the performance

idual troubleshooting tests that require the following topics:

rd Replacement



8oubleshooting This section describes service event action, and provides a separate troubinspection procedure (PIP) and indivoperator interpretation. Choose from

Processing Service CodesTroubleshooting ChartService Code Categories Service Code TableService IndicatorDevice User TestDevice Printed Circuit Boa


LIF Troubleshooting

P

In fails to execute properly, a service code is turns ON. Service codes rarely occur and ualified service personnel before the

Always complete the performance ntering and clearing any service code(s).

og may not necessarily indicate a dicate transient electromagnetic charge (ESD). If you suspect transient

clear the service code(s), and cycle the occur, it may have been the result of EMI

PrCo and consult the Troubleshooting Chart.

ce Log. Record the service code(s), ce code extension.g, and then turn the device OFF.


6-2



rocessing Service Codes

troduction When an internal program or process logged and the service indicator LED should be investigated thoroughly by qdevice is placed back into active use. inspection procedure (PIP) after encouService codes stored in the Service Lpermanent error. Service codes can ininterference (EMI) or electrostatic disEMI or ESD as the source of an error,power. If the service code does not reor ESD.

ocessing Service des

To process service code(s):1. Note any problems with the device2. Review service codes in the Servi

including the date, time, and servi3. Select CLEAR LOG in the service lo


LIF Troubleshooting

P

PrCo

tion procedure (PIP). device may be returned to regular use. e been related to EMI or ESD.) any time during the PIP, stop the PIP and s procedure.rt for the suggested corrective action for

nd then locate the service code in the

Code Categories table to quickly jump to de Table.e corrective action calls for the k in the Troubleshooting Chart or click the bottom of the Service Code Table pages cess. inputs, and then repeat the PIP. your local Physio-Control service or sales

6-3



rocessing Service Codes (continued)

ocessing Service des (continued)

4. Complete the performance inspec– If completed successfully, the

(The service code(s) may hav– If the service LED turns ON at

continue to the next step in thi5. Consult the Troubleshooting Cha

your PIP failure. -OR-Review the Service Log codes, aService Code Table.Note: Use the links in the Servicethe correct code in the Service Co

6. Read the corrective action(s). If threplacement of a part, click the linappropriate part in the footer at theto jump to the corrective action pro

7. Service the device based on these8. For persistent error codes, contact

representative.


LIF Troubleshooting

TrA rective Action

Ph en or replace loose items.ce broken components.

l cleaning.

mer keypad.t identification label.on/hazard label.ng instruction label.

Po to ac power source.s Alert alarm.


6-4



oubleshooting Chart rea Observed Symptom Suggested Cor

ysical Inspection Loose or broken hardware Locate and tightLocate and repla

Evidence of dirt, fluids, or foreign objects

Perform externa

Damaged keypad or labels Replace elastoReplace producReplace explosiReplace operati

wer Off Device beeps when turned off

Connect device Disable AC Los


LIF Troubleshooting

TrA orrective Action

Po ace the W18 UI Flex Cable.ace the A05 UI PCB.A04 Therapy PCB.

A01 System PCB.

ace the W18 UI Flex Cable.A01 System PCB.

A05 UI PCB.

essing Service Codes for assistance.

tenance Prompt interval.intenance Prompt interval.

Ke ad test.ace the elastomer keypad.A05 UI PCB.

ad test.ace standard paddles.ace the W01 Therapy Connector.A04 Therapy PCB.


6-5



oubleshooting Chart (continued) rea Observed Symptom Suggested C

wer On Display on, no power-on LED Check or replCheck or replReplace the

Continuous reset Replace the Frozen at the power-on screen Check or repl

Replace the Distorted display Replace the Service indicator remains on Refer to ProcMAINTENANCE DUE message remains on screen

Set the MainReset the Ma

ypad Improper button response Perform keypCheck or replReplace the

Standard paddle buttons Perform keypCheck or replCheck or replReplace the


LI Troubleshooting

TA rrective Action

P test.r paper. on pins 14 and 16 on the J38 test he A05 UI PCB.igher than 3.3 V, replace the W14 Printer .ower than 3.3 V: r replace the A12 Printer Assembly. the A05 UI PCB.

per paper. Printer Flex Cable connection.e the A05 UI PCB.

per paper.ead.e the A12 Printer Assembly.


6-6



roubleshooting Chart (continued) rea Observed Symptom Suggested Co

rinter Not printing Perform printer Check for propeCheck for 3.3 Vconnector on t■ If either is h

Flex Cable■ If both are l

– Check o– Replace

Light print Verify use of proCheck the W14Check or replac

Missing or broken characters Verify use of proClean the printhCheck or replac


LIF Troubleshooting

TrA rrective Action

Au ce tone test.ker connection.e the W02 Speaker Assembly.e the A01 System PCB.

Pom

7 Battery.e the A03 Power Module.

Then

ith proper test load shorting.y of the test plug or shorting bar.y of the QUIK-COMBO cable.e the W01 Therapy Connector.4 Therapy PCB.

lator calibration.

Pach

e the A14 Inductive Resistor (less than

e the A04 Therapy PCB.1 System PCB.


6-7



oubleshooting Chart (continued) rea Observed Symptom Suggested Co

dio Inaudible or garbled audio Perform the voiCheck the speaCheck or replacCheck or replac

wer source anagement

No backup battery operation Replace the A0Check or replac

erapy - delivered ergy

Unable to complete auto test or user test

Rerun the test wCheck continuitCheck continuitCheck or replacReplace the A0

Delivered energy out of tolerance

Perform defibril

tient impedance annel broken

Abnormal energy delivery Check or replac5 ohms).Check or replacReplace the A0


LIF Troubleshooting

TrA rective Action

Pach(c

0 ohm load during 3:00 AM test, rerun test plug.omplete PIP.ace the A01 System PCB.

of the QUIK-COMBO cable; replace if

of the W01 Therapy Connector; sary.1 System PCB.

Thca

e the Therapy cable.e the W01 Therapy Connector.1 System PCB.

ECG signal.e the ECG cable.e the W06 ECG connector.e the A02 Patient Parameter PCB.1 System PCB.


6-8



oubleshooting Chart (continued) rea Observed Symptom Suggested Cor

tient impedance annel broken ontinued)

Low patient impedance If tested into a 5test with correctIf test passes, cIf test fails, repl

Therapy cable leads off (QUIK-COMBO only)

Check continuitynecessary.Check continuityreplace if necesReplace the A0

erapy - Synchronous rdioversion

No paddles channel sync mark

Check or replacCheck or replacReplace the A0

No lead channel sync mark Check for noisyCheck or replacCheck or replacCheck or replacReplace the A0


LIF Troubleshooting

TrA rective Action

Thca

ker placement on R-wave.pad test.eplace the A05 UI PCB.s, run the user test and troubleshoot error

Pach

urer configuration bit setting. test:heck key tactile feedback. the elastomer keypad. the A05 UI PCB.s, follow error code procedure.

e the A04 Therapy PCB.

EC e the ECG cable.e the W06 ECG Connector.2 Patient Parameter PCB.


6-9




erapy - Synchronous rdioversion (continued)

Failure to transfer coincident with sync mark

Check sync marPerform the key■ If test fails, r■ If test passe

code.

cer option aracteristics

Pacer does not turn on Verify manufactPerform keypad■ If test fails, c

– Replace– Replace

■ If test passe

Pacing current/rate out of tolerance

Check or replac

G lead characteristics No ECG Check or replacCheck or replacReplace the A0


LIF Troubleshooting

TrA rrective Action

EC(c

e the ECG cable.2 Patient Parameter PCB.

r output.e the ECG cable.e the A02 Patient Parameter PCB.

Thle

r output.e the therapy cable.e the A01 System PCB.

r output.display.G out connector.

Re sync function.t/Sync In connector. If bad, replace the dule.e the W09 Power Cable.e the A01 System PCB.e the A03 Power module.


6-10



oubleshooting Chart (continued)

rea Observed Symptom Suggested Co

G lead characteristics ontinued)

No amplitude ECG Check or replacReplace the A0

ECG gain out of tolerance Check simulatoCheck or replacCheck or replac

erapy - Paddle ECG ad characteristics

ECG gain out of tolerance Check simulatoCheck or replacCheck or replac

ECG analog out (missing or out of tolerance)

Check simulatoCheck ECG on Check W11 EC

mote sync No remote sync Turn on remoteCheck ECG OuA03 Power moCheck or replacCheck or replacCheck or replac


LIF Troubleshooting

TrA rective Action

O e the SpO2 cable.e the SpO2 sensor.e the W05 SpO2 Assembly.

e the SpO2 cable.e the SpO2 sensor.e the W05 SpO2 Assembly.e the A06 OEM PCB.

Sp e the W04 Speed Dial Assembly.5 UI PCB.

Nto

figuration setting.3 Power module.

G e the power cord.3 Power module.

Le 3 Power module.

6-11




ximeter No SpO2 response (no cable detected)

Check or replacCheck or replacCheck or replac

Saturation reading missing or out of tolerance

Check or replacCheck or replacCheck or replacCheck or replac

eed Dial Speed Dial not functioning Check or replacReplace the A0

o ac power reminder ne

No alert Check user conReplace the A0

rounding resistance Fails ground resistance test Check or replacReplace the A0

akage current Fails chassis leakage test Replace the A0


LIF Troubleshooting

S

Co l format:

In d Assemblies

0x1x erapy, A05 UI, A12 Printer,

ble, W18 UI Flex Cable 2x3x4x erapy, A05 UI,

50 PCB, A04 Therapy, A05 UI,

51 A04 Therapy, A07 Battery,

6x EM PCB, A10 SpO2 Module 8x PCB 9x wer Module, A04 Therapy, A07 Batteryaxbx

6-12



ervice Code Categories

des are organized into the following categories, in four-digit hexadecima

itial Digit Category Description Associated PCBs an

xx UT Utilities A01 System xx UI User Interface A01 System, A04 Th

W14 Printer Flex Caxx DC Data Communications A01 System xx DM Data Management A01 System xx SM System Monitor A01 System, A04 Th

W18 UI Flex Cable xx PC Processor Control A01 System, A02 PP

W18 UI Flex Cable xx PM Power Management A03 Power Module,

W08 Battery Cable xx PP Patient Parameter – SpO2 A02 PP PCB, A06 Oxx DSP Digital Signal Processor A01 System, A02 PPxx TH Therapy A01 System, A03 Poxx PR Printer A12 Printer xx BM Behavior Manager A01 System


LIF Troubleshooting

SC ive Action

00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB00 the A01 System PCB10 lace the W18 UI Flex Cable

lace the A05 UI PCBlace the A01 System PCB

10 ad the device software*lace the A01 System PCB

orced update mode (Continued on next page)

W18 UI Flex Cable

6-13



ervice Code Table

ode Service Code Description Correct

02 System Flash memory voltage error Replace03 Cannot erase system Flash memory Replace04 Cannot write to system Flash memory Replace06 System ADC read error Replace07 System DAC not responding Replace08 ECG OUT DAC self-test failed Replace0a System ADC background test failed Replace0b System ADC failed self-calibration Replace0c System Flash memory ID unknown Replace0d System hardware/software configuration lost Replace0e UI – system communication lost 1. Rep

2. Rep3. Rep

0f Display update timer error 1. Relo2. Rep

* Use software loader tool in f

A01 System PCB A05 UI PCB


LIF Troubleshooting

SC ive Action Code10 ad the device software*

lace the A01 System PCB10 lace the W18 UI Flex Cable

lace the A05 UI PCB10 ad the device software*

lace the A01 System PCB10 r error and perform PIP

lace the W18 UI Flex Cable1c the A05 UI PCB1c the A05 UI PCB1c ad the device software*

lace the A05 UI PCB1c the A05 UI PCB


W18 UI Flex Cable

6-14



ervice Code Table (continued)

ode Service Code Description Correct10 Display update queue error 1. Relo

2. Rep13 System detected unexpected UI reset 1. Rep

2. Rep14 Voice prompt/audio watchdog failure 1. Relo

2. Rep15 USB data time-out error 1. Clea

2. Rep01 UI FPGA programming error Replace02 UI FPGA verification error Replace03 UI FPGA program file error 1. Relo

2. Rep04 UI ADC not functioning Replace

A01 System PCB A05 UI PCB


LIF Troubleshooting

SC tive Action1c ck the W14 Printer Flex Cable

lace the A12 Printerlace the A05 UI PCB

1c ck the W14 Printer Flex Cablelace the A12 Printerlace the A05 UI PCB

1c the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB


A05 UI PCB

6-15




ode Service Code Description Correc05 Printer ADC out of tolerance (temperature) 1. Che

2. Rep3. Rep

06 Printer ADC out of tolerance (voltage) 1. Che2. Rep3. Rep

07 UI voltage out of tolerance (5 V) Replace08 UI voltage out of tolerance (3.3 V) Replace09 UI voltage out of tolerance (2.5 V) Replace0a UI voltage out of tolerance (35 V) Replace0b UI voltage out of tolerance (SW VBATT) Replace0c UI voltage out of tolerance (ground) Replace0f UI hardware I.D. corrupted Replace10 UI boot program corrupted Replace

W14 Printer Flex Cable A12 Printer


LIF Troubleshooting

S


A05 UI PCB

C ive Action1c ad the device software*

lace the A05 UI PCB1c ad the device software*

lace the A05 UI PCB1c ad the device software*

lace the A05 UI PCB1c the A05 UI PCB1c the A05 UI PCB1f n required; refer to error code logged

fff.20 the A01 System PCB20 ad the device software*

lace the A01 System PCB

6-16




A01 System PCB

ode Service Code Description Correct11 UI application Flash memory corrupted 1. Relo

2. Rep12 UI font Flash memory corrupted 1. Relo

2. Rep13 UI FPGA Flash memory corrupted 1. Relo

2. Rep16 UI CPU RAM test failed on power-on Replace17 UI CPU RAM test failed during normal operation Replaceff Additional information related to error code that is

logged before 1fffNo actiobefore 1

04 System cannot initialize serial port (system connector) Replace05 System cannot initialize driver for serial port (system

connector)1. Relo2. Rep


LIF Troubleshooting

SC tive Action30 oad the device software*

lace the A01 System PCB30 ar memory (service mode)

oad the device software*lace the A01 System PCB

30 ar memory (service mode)oad the device software*lace the A01 System PCB




6-17




ode Service Code Description Correc01 System cannot use data management (DM) Flash

memory1. Rel2. Rep

02 System data management Flash memory corrupted 1. Cle2. Rel3. Rep

05 System cannot delete DM record 1. Cle2. Rel3. Rep

07 System cannot create new DM record 1. Cle2. Rel3. Rep

08 System could not store DM record 1. Cle2. Rel3. Rep

A01 System PCB


LIF Troubleshooting

S


C tive Action30 ar memory (service mode)

oad the device software*lace the A01 System PCB

30 oad the device software*lace the A01 System PCB



30 the A01 System PCB3f n required; refer to error code logged

fff.

6-18




A01 System PCB

ode Service Code Description Correc09 System could not erase oldest DM record 1. Cle

2. Rel3. Rep

0a System cannot clear DM memory 1. Rel2. Rep

0b System error writing DM record 1. Cle2. Rel3. Rep

0c System cannot read archived DM record 1. Cle2. Rel3. Rep

10 System error DM memory corrupt Replaceff Additional information related to error code that is

logged before 3fffNo actiobefore 3


LIF Troubleshooting

SC ive Action40 lace the coin cell battery

ad the device software*lace the A01 System PCB





40 ck coin-cell batteryror still occur, Replace A01 System PCB

40 the A01 System PCB40 the A01 System PCB


Coin Battery

6-19




ode Service Code Description Correct05 System NVRAM error log 1. Rep

2. Relo3. Rep

06 Error log queue not functioning 1. Relo2. Rep

08 Error log count corrupted 1. Relo2. Rep

09 System RAM test failed 1. Relo2. Rep

0a System program Flash memory corrupted 1. Relo2. Rep

0b Program contents failure 1. Che2. If er

0c System ADC voltage low Replace0d System ADC voltage high Replace

A01 System PCB


LIF Troubleshooting

SC ive Action40 lace the W18 UI Flex Cable

lace the A05 UI PCBlace the A04 Therapy PCB

40 the device software*40 the device software*4f n required for 4fff; refer to error code

before 4fff.50 the A01 System PCB50 ad the device software*

lace the A01 System PCB50 the A01 System PCB50 the A01 System PCB50 ad the device software*

lace the A01 System PCB50 the A01 System PCB


A CB W18 UI Flex Cable

6-20




ode Service Code Description Correct10 Service LED failed 1. Rep

2. Rep3. Rep

12 Voice Flash memory corrupted Reload 13 Voice/font Flash memory invalid Reload

ff Additional information related to error code that is logged before 4fff

No actiologged

03 System watchdog failed Replace04 System watchdog reset 1. Relo

2. Rep05 System CPU error during boot-up Replace06 System RAM failed during boot-up Replace07 System checksum failure during boot-up 1. Relo

2. Rep08 System boot program failure Replace

01 System PCB A04 Therapy PCB A05 UI P


LIF Troubleshooting

SC ive Action50 ad the device software*

lace the A01 System PCB50 lace the coin cell battery

lace the A01 System PCB50 ad the device software*




lace the A01 System PCB50 the coin cell battery


Coin Battery

6-21




ode Service Code Description Correct09 Real-time clock (RTC) access failed 1. Relo

2. Rep0a Coin cell battery not detected 1. Rep

2. Rep0b Cannot use system NVRAM 1. Relo

2. Rep0c System application start error 1. Relo

2. Rep0d System software initialization time out 1. Relo

2. Rep0e System application start error 1. Relo

2. Rep10 Configuration mismatch Replace

A01 System PCB


LIF Troubleshooting

SC ive Action50 lace the coin cell battery

ad the device software*50 the coin cell battery50 the device software*50 the coin cell battery50 the A01 System PCB50 the A01 System PCB50 the A01 System PCB50 the A01 System PCB50 the coin cell battery50 the coin cell battery50 lace the coin cell battery

lace the A01 System PCB


Coin Battery

6-22




ode Service Code Description Correct11 NVRAM configuration data error 1. Rep

2. Relo12 Configuration data error Replace13 System meter initialization error Reload 14 System meter mismatch Replace15 NVRAM error Replace16 MFG data mismatch Replace17 NVRAM MFG data lost Replace18 Watchdog reset failed Replace19 NVRAM corrupted Replace1a NVRAM corrupted Replace1c RTC not running 1. Rep

2. Rep

A01 System PCB


LIF Troubleshooting

S


Coin Battery

C n50 oin cell battery

01 System PCB50 software*50 software*50 software*50 software*50 software*50 software*50 software*50 cell battery50 d perform PIP

01 System PCB50 d perform PIP

02 PP PCB

6-23




A01 System PCB A02 PP PCB

ode Service Code Description Corrective Actio1d RTC out of sync 1. Replace the c

2. Replace the A1e System software execution error Reload the device1f System software read error Reload the device20 System software write error Reload the device21 System software error Reload the device22 System software exception code Reload the device23 System software exception code Reload the device24 System software exception code Reload the device26 NVRAM low battery interrupt Replace the coin 27 System USB did not initialize 1. Clear error an

2. Replace the A28 PP USB did not initialize 1. Clear error an

2. Replace the A


LIF Troubleshooting

S


A A02 PP PCB W18 UI Flex Cable

C ive Action50 r error and perform PIP

lace the A04 Therapy PCB50 r error and perform PIP

lace the W18 UI Flex Cablelace the A05 UI PCB

50 r error and perform PIPlace the A01 System PCB

50 ck configuration codedevice type (software loader program)lace the A01 System PCB

50 r error and perform PIPlace the A02 PP PCB

50 r error and perform PIPlace the W18 UI Flex Cablelace the A05 UI PCB

6-24




04 Therapy PCB A01 System PCB A05 UI PCB

ode Service Code Description Correct29 Therapy USB did not initialize 1. Clea

2. Rep2a UI USB did not initialize 1. Clea

2. Rep3. Rep

2b USB system failed 1. Clea2. Rep

2f Device type invalid 1. Che2. Set 3. Rep

30 PP USB disconnect 1. Clea2. Rep

31 UI USB disconnect 1. Clea2. Rep3. Rep


LIF Troubleshooting

S


y PCB A05 UI PCB

C e Action

50 error and perform PIPce the A04 Therapy PCB

50 error and perform PIPd the device software*

50 error and perform PIPd the device software*ce the A01 System PCB

50 error and perform PIPd the device software*ce the A01 System PCB

50 he A01 System PCB

50 error and perform PIPce the A02 PP PCBce the A01 System PCB

6-25




A01 System PCB A02 PP PCB A04 Therap

ode Service Code Description Correctiv

32 Therapy USB disconnect 1. Clear 2. Repla

33 PP USB download time out 1. Clear 2. Reloa

36 USB initialization failed 1. Clear 2. Reloa3. Repla

37 USB unitization error 1. Clear 2. Reloa3. Repla

38 Cannot clear interrupt source Replace t

39 Bus error reported by USB PP channel 1. Clear 2. Repla3. Repla


LIF Troubleshooting

S


A07 Battery

C ive Action

50 r error and perform PIPlace the A05 UI PCBlace the A01 System PCB

50 r error and perform PIPlace the A04 Therapy PCBlace the A01 System PCB



50 the A01 System PCB

6-26




A01 System PCB A03 Power Module


3a Bus error reported by USB UI channel 1. Clea2. Rep3. Rep

3b Bus error reported by USB therapy channel 1. Clea2. Rep3. Rep

3c USB host driver cannot create transfer descriptor 1. Clea2. Rep

3d USB host driver received message larger than maximum allowed

1. Clea2. Rep

40 Inconsistent RTC time Replace


LIF Troubleshooting

S


A07 Battery

C ive Action

51 lace the A07 Batterylace the A03 Power module

51 wer supply voltage is <14 Vdc, replace Power module4 Vdc, clear error and perform PIP

51 the A03 Power module






51 the A07 Battery

6-27




A03 Power Module A04 Therapy PCB


05 Battery failed to reach charge in 2.5 hours 1. Rep2. Rep

06 Power supply out of tolerance 1. If poA03

2. If >1

07 Power module RAM error Replace

08 Power module self-test service code Replace

0a Battery <10 V after 20 minutes of charging 1. Rep2. Rep

0b Does not switch to battery power Replace

0c Does not detect ac disconnect Replace

0d Battery powered when connected to ac power Replace

0e Battery <10 V after charge cycle Replace


LIF Troubleshooting

S


A07 Battery

C ive Action

51 ck battery connectionlace the A07 Batterylace the A03 Power module


51 ck the A07 Battery connectionck W08 Battery Cableck for valid power hardware ID in VICE/STATUS/DEVICE DATA overlaylace the A07 Batterylid power hardware ID; replace the Power module power hardware ID; replace the Therapy PCB

6-28




A03 Power Module


0f Battery charge cycle stopped 1. Che2. Rep3. Rep

10 AC isolation diode shorted Replace

12 Battery not detected 1. Che2. Che3. Che

SER4. Rep5. Inva

A036. Valid

A04


LIF Troubleshooting

S


A02 PP PCB

C ive Action

51 A07 Battery (LIFEPAK 20e)asurement of white wires of A07 Battery thermistor LIFEPAK 20)lace the A07 Battery if <400 Ohmslace the A03 Power module if >400 Ohms



51 the A07 Battery

51 the A07 Battery

5f n required for 5fff; refer to error code efore 5fff

6-29




A06 OEM PCB


15 Battery thermistor <400 Ohms ReplaceOhm me(battery ■ Rep■ Rep

16 Charger reporting zero during battery charging Replace

17 No 12C connection detected (LIFEPAK 20e only)

1. Rep2. Rep

18 Power module connected to NiMH battery(LIFEPAK 20 only)

Replace

1a Battery failure Replace


No actiologged b


LIF Troubleshooting

S


10 SpO2 Module

C ive Action

60 the device software*




60 ck configurationad the device software*

60 ad the device software*lace the A02 PP PCB

60 ck configurationad the device software*


60 the A06 OEM PCB

60 the A06 OEM PCB

6-30




A02 PP PCB A


02 PP program corrupted Reload

03 PP program not found Reload

04 PP boot-up error Reload

09 No PP data Reload

0c SpO2 misconfigured 1. Che2. Relo

0e PP reset 1. Relo2. Rep

0f OEM configuration error 1. Che2. Relo

10 PP initialization error Reload

18 Incorrect updated SpO2 image Replace

19 Incorrect updated SpO2 image CRC Replace


LIF Troubleshooting

S


C tive Action

68 e the A02 PP PCB

68 ar error and perform PIPlace the A02 PP PCB





68 e the A10 SpO2 Module

6f on required for 6fff; refer to error logged 6fff.

6-31




A01 System PCB

ode Service Code Description Correc

01 PP power supply out of tolerance Replac

02 PP pre-amp data invalid 1. Cle2. Rep

04 PP data RAM test error 1. Cle2. Rep

05 PP RAM test error 1. Cle2. Rep

06 PP CRC test error 1. Cle2. Rep

07 PP ECG test error 1. Cle2. Rep

0b SpO2 board error Replac


No actibefore


LIF Troubleshooting

S


A04 Therapy PCB

C tive Action




80 ar error and perform PIPlace the A01 System PCB



81 un the user testlace the A01 System PCB

81 form TCP - defibrillator calibrationlace the A01 System PCB

6-32




A01 System PCB A07 Battery

ode Service Code Description Correc

0a System DSP error Reload

13 Voice format error Reload

14 No paddles data 1. Rel2. Rep

1b DSP did not receive USB SOF (start of frame) interrupt 1. Cle2. Rep

05 Impedance channel out of calibration Replace

08 Paddles data out of sync 1. Rel2. Rep

09 Paddles pre-amp user test failed 1. Rer2. Rep

0b Real impedance <-30 ohms for one second 1. Per2. Rep


LIF Troubleshooting

S


A04 Therapy PCB

C ive Action

8f n required for 8fff; refer to error logged fff.




90 the A07 Battery


90 ck the stack connectorlace the A04 Therapy PCB

90 ad the device software*lace the A04 Therapy PCB



6-33




A01 System PCB



No actiobefore 8

04 Unable to initialize therapy control Replace

05 Defib disabled Replace

07 Shock not delivered Reload

09 Defib charge time expired Replace

0b Pacing rate out of tolerance Replace

0f Unable to initialize therapy control 1. Che2. Rep

11 Pacer fault 1. Relo2. Rep

17 Pacer disabled Reload

1a Pacer rate storage corrupted Reload


LIF Troubleshooting

S


Therapy PCB

C ive Action

90 ck the stack connectorlace the A04 Therapy PCB



9c the A04 Therapy PCB

9c the A01 System PCB

9c r error and perform PIPlace the A04 Therapy PCB

9c orm TCP - defibrillator calibrationr Service Log


6-34




A03 Power Module A04


1b Therapy PCB communication lost 1. Che2. Rep

1d Testing purpose only Replace

21 Impedance value indicates regulator in System PCB pre-amp failed

1. Clea2. Rep

03 Therapy processor, unplanned reset Replace

04 Therapy/system controller communication watchdog Replace

05 CRC error 1. Clea2. Rep

06 Calibration constant A out of range 1. Perf2. Clea

07 Calibration constant B out of range 1. Perf2. Clea


LIF Troubleshooting

S


Therapy PCB

C ive Action

9c ad the device software*lace the A04 Therapy PCB






9c ck power module 26-pin ribbon cable to or A04 Therapy PCBlace the A03 Power modulelace the A04 Therapy PCB



6-35




A01 System PCB A04


08 Therapy ROM cyclic redundancy check (CRC) failed 1. Relo2. Rep

09 Therapy RAM pattern write test failed Replace

0a Therapy relay idle coil voltage out of range Replace

0b Therapy relay enabled coil voltage out of range (5 ms) Replace

0c Therapy relay enabled coil voltage out of range (100 ms)

Replace

0d Therapy relay drive enabled coil voltage out of range Replace

0f Therapy/power assembly communication error 1. CheJ16

2. Rep3. Rep

11 Capacitor Dump failed Replace

12 Therapy PCB 5 V out of range Replace


LIF Troubleshooting

S


C ive Action











6-36




A04 Therapy PCB


13 Therapy PCB 15 V out of range Replace

14 Therapy PCB -15 V out of range Replace

15 Therapy ADC time out error Replace

18 3:00 AM H bridge test: NE leg shorted Replace

19 3:00 AM H bridge test: SE leg shorted Replace

1a 3:00 AM H bridge test: NW leg shorted Replace

1b 3:00 AM H bridge test: SW leg shorted Replace

1c 3:00 AM H bridge test: east side stuck open Replace

1d 3:00 AM H bridge test: west side stuck open Replace

1e 3:00 AM H bridge test: charge time out of range 1. Perf2. Clea


LIF Troubleshooting

S


C ive Action

9c ctive resister is not connected or is openlace the A04 Therapy PCBlace the A01 System PCB










6-37




A04 Therapy PCB


1f 3:00 AM shorted paddles relay contact test: relay shorted

1. Indu2. Rep3. Rep

20 3:00 AM shorted paddles relay contact test: relay shorted

Replace

21 3:00 AM pace drive test: pace power supply stuck on Replace

22 3:00 AM pace drive test: pace power supply inoperable Replace

23 3:00 AM pace drive test: relay contacts shorted Replace

24 3:00 AM pace drive test: relay drive low side shorted Replace

25 3:00 AM pace drive test: relay drive high side shorted Replace

26 3:00 AM pace drive test: pace FET shorted Replace

27 3:00 AM pace drive test: pace current path open Replace

28 3:00 AM pace drive test: pace set point error Replace


LIF Troubleshooting

S


C ive Action










9c rgy capacitor is not connected or is openlace the A04 Therapy PCB


6-38




A04 Therapy PCB


29 3:00 AM redundant controls test: redundant controls stuck on

Replace

2a 3:00 AM redundant controls test: enable 2 stuck on Replace

2b 3:00 AM redundant controls test: enable 1 stuck on Replace

2c Capacitor voltage per pacing pulse too high Replace

2d Capacitor current per pacing pulse too high Replace

2e Cap current per pacing pulse too high Replace

2f Pacing current and selected current out of range Replace

30 Pacing pulse width too short Replace

31 Pacing pulse width too long Replace

32 Capacitor voltage and predicted capacitor voltage mismatch

1. Ene2. Rep

35 Therapy CPU instruction test failed Replace


LIF Troubleshooting

S

C ive Action

9c the device software*





6-39




A04 Therapy PCB


36 Therapy software stack overflow Reload

3a Energy capacitor overvoltage error Replace

3b 3:00 AM redundant controls test: charge rate stuck on Replace

3e Therapy software error Replace

3f Therapy software error Replace


LIF Troubleshooting

SC ive Action

a0 r error and perform PIPad the device software*

a0 he device software*

b0 r error and perform PIPlace A01 System PCB

b0 he device software*






b0 r error and perform PIP. lace A01 System PCB.


6-40



ervice Code Table (continued) ode Service Code Description Correct

0b Printer communication lost 1. Clea2. Relo

0e Printer initialization error Reload t

01 Invalid state request 1. Clea2. Rep

11 System behavior manager error Reload t

12 Energy cap charging time out Reload t

13 Shock advisory system error Reload t

14 Shock advisory system time out Reload t

16 Motion detect timer error Reload t

17 Shock result time out Reload t

18 USB interrupt error 1. Clea2. Rep

A01 System PCB


LIF Troubleshooting

U

AcSt

s options that provide information such as rrors, and counters for shock and pacing

nu, access the SERVICE menu and select

s log

nters

ement memory


6-41



sing the Service/Status Features

cessing the Service/atus Features

The SERVICE/STATUS submenu includestored manufacturing data, recorded eoperation.To display the SERVICE/STATUS submeSTATUS.The SERVICE/STATUS options include:

Option Description

Device Log Show device statu

Device Data Show device data

Service Log Show service log

Counters Display shock cou

Clear Memory Clear data manag


LIF Troubleshooting

U

De ATUS submenu to view essential device rating software was installed, and as the shock count.ing information:

en the device was manufactured, hen the operating software was loaded.

ether there are any error codes stored in og (refer to Processing Service Codes).

of times the device has been powered on.

pulses delivered by the device.

e device defibrillation capacitor has been

power-on time.

running time.

unning time.


6-42



sing the Service/Status Features (continued)

vice Log Select DEVICE LOG on the SERVICE/STcharacteristics, such as when the opeaccumulative device operations, suchThe device log data includes the follow

Data Description

Manufacturing date The date whspecifically, w

Fault Messages Indicates whthe Service L

Power Cycle Count The number

Pacing Count Total pacing

Shock Count Total times thcharged.

Power On Time Total device

Printer On Time Total printer

SpO2 Operating Time Total SpO2 r


LIF Troubleshooting

U

De TATUS submenu to view essential device ber, and accumulative device operations,

l number

number

was built

mbly hardware serial number

mbly software version number

meter PCB hardware serial number

meter PCB software version number

ardware serial number

troller hardware serial number


6-43




vice Data Select DEVICE DATA on the SERVICE/Scharacteristics, such as the serial numsuch as the shock count.The device data includes:

Data Description

Serial Number Device seria

Dash Number Device dash

Manufacture Date Date device

Power HW Power asse

Power SW Power asse

PP HW Patient para

PP SW Patient para

OEM HW OEM PCB h

SC HW System con


LIF Troubleshooting

U

De(c

troller software version number

troller voice prompt version

B hardware serial number

B software version number

ce hardware serial number

ce software version number

ce field programmable E program

are serial number

re version number


6-44




vice Data ontinued) Data Description

SC SW System con

SC Voice System con

Therapy HW Therapy PC

Therapy SW Therapy PC

UI HW User interfa

UI SW User interfa

UI FPGA User interfa

SpO2 HW SpO2 hardw

SpO2 SW SpO2 softwa


LIF Troubleshooting

U

Se ATUS submenu to view the device service

information:

entries (service codes)

rvice log

ervice log


6-45




rvice Log Select SERVICE LOG on the SERVICE/STrecord.The service log includes the following

Data Description

Service dates Service log

PRINT LOG button Prints the se

CLEAR LOG button Clears the s


LIF Troubleshooting

U

Co TUS submenu to view the joule settings, ince the last reset, and the total number of t into operation.L. This resets the boxed subtotal counters can also reset the counters using the the next page.


6-46




unters Select COUNTERS on the SERVICE/STAthe total number of shocks delivered sshocks delivered since the device wenTo reset the counters, select CLEAR ALbut not the running-total counters. YouCLEAR MEMORY feature discussed on


LIF Troubleshooting

U

Cl /STATUS submenu to clear the flash data ory PCB. A count-down timer appears to

quires approximately 30 seconds.

(up to 45 minutes of first-in-first-out ermanently deleted.t reports are permanently deleted.hen the device is placed into new or

s no longer required. The data as part of some service actions.t memory is permanent; there is no undo. before clearing the memory, print the the Data Management section in the

6-47




ear Memory Select CLEAR MEMORY on the SERVICEmanagement memory on the A02 Memindicate the clearing process, which reSpecifically, it clears the following:■ ECG data — All stored ECG data

continuous ECG waveforms) are p■ Patient reports — All stored patienClear the data management memory wdifferent use and the old patient data imanagement memory is also cleared Note: Clearing the data managemen

To save important patient dataindividual patient data (refer tooperating instructions.


LIF Troubleshooting

S

icate the presence of errors in the Service ates when a service code is written to the vice Codes to resolve the problem.uminates when you turn on the device, a ervice Log. If you cycle the power, and the gain, it does not mean that there are no view the Service Log and resolve the the first instance.

6-48



ervice Indicator

The service indicator LED does not indLog. The service indicator LED illuminService Log. Refer to Processing SerFor example, if the service indicator illservice code has been written to the Sservice indicator does not illuminate acodes in the Service Log. You must reservice code that was written there in


LIF Troubleshooting

D

of self-tests occur. If errors are detected, Self-testing does not occur only at vice is turned on.cting USER TEST does not initiate a est status and produces reports. The le is complete and then reports USER TEST

NS/USER TEST feature. This operation efibrillator capacitor to 10 joules and then oes not pass, the service indicator LED e Service Log (refer to Processing

6-49



evice User Test

When you turn on the device, a seriesthe service indicator LED illuminates. power-on; it is continuous while the dePressing the OPTIONS button and seleself-test cycle; rather, it monitors self-tdevice waits until the next self-test cycPASSES. One operation is specific to the OPTIOconsists of one cycle of charging the ddumping the charge. If this operation dilluminates and an error is written to thService Codes).


LIF Troubleshooting

D

is replaced, then reloading of device is required. le software programs maintained on the efibrillator/monitor, know as a device

is documented as a single software software will maintain the device at a re set.sing the LIFENET System Asset ur local Physio-Control service or sales

6-50



evice Printed Circuit Board Replacement

Anytime a printed circuit board (PCB) system software to the current versionThe device system software are multipcircuit boards within the LIFEPAK 20 dsoftware set. This device software setversion and part number. Updating theknown released device system softwaDevice Software set can by install by umanagement tools or by contacting yorepresentative.



PM

d testing of the device helps detect and anical problems. When scheduled e MAINTENANCE DUE message displays for the device is turned on (if a maintenance aintenance interval, refer to Setting a esetting the Maintenance Prompt.

topics, refer to Battery Maintenance. The e following:

uidelines



9reventive aintenance

Periodic maintenance, inspection, anprevent possible electrical and mechmaintenance is due for the device, thapproximately 10 minutes each time interval is set). To set and reset the mMaintenance Prompt Interval and RFor information about battery-relatedinformation in this section includes th

Maintenance and Testing GCleaningDevice Useful LifeSupport PolicyStoring the DeviceRecycling


LIF Preventive Maintenance

M

d testing of the device will help prevent oblems. Refer to the Operator Checklist in al items.le for preventive maintenance activities.

regular intervals, refer to scheduled

As Needed Scheduled

re (PIP) X Annually

TCP) X

X

X

X

X

5 years

life X

7-2



aintenance and Testing Guidelines

Periodic maintenance, inspection, anpossible electrical and mechanical prthe operating instructions for additionThe following table shows the scheduFor items that should be replaced at replacement Items shown below.

Activity

Performance inspection proceduTest and calibration procedures (Exterior physical inspectionInterior Physical InspectionExterior cleaningInterior cleaningCoin battery replacementA07 battery replacement (serviceminimum of 2 years)



C

ClM

need to perform an external and internal w.

Description

Grounded conductive surfaceand wrist strap

Nonmetallic

Clean and lint-free

Clean and dry (60 psi, maximum)

7-3



leaning

eaning Tools and aterials

The tools and materials that you will cleaning of the device are listed belo

Product

Static-discharge-protected work area

Isopropyl alcohol

Quaternary ammonium compounds

Peroxide (peracetic acid) solutions

Cotton swabs

Vacuum cleaner

Soft-bristle brush

Cloth

Compressed air



C

ExPr rse or soak any portion of this device in

ling any fluid on the device or

n any part of this device or accessories enolic compounds. Do not use abrasive ot attempt to sterilize this device or any

cified in the accessory operating

iping the surface with any of the following

ds

s

7-4



leaning (continued)

ternal Cleaning ocedure

WARNING!Shock or fire hazard. Do not immewater or any other fluid. Avoid spilaccessories.

CAUTION!Possible case damage. Do not cleawith bleach, bleach dilution, or phor flammable cleaning agents. Do naccessories unless otherwise speinstructions.

Clean the exterior of the device by wsolutions:■ Soap and water■ Quaternary ammonium compoun■ Isopropyl alcohol■ Peroxide (peracetic acid) solution



C

SpPr

t it from the patient cable and clean the propyl alcohol pad. Allow the sensor to dry

ith a 70% isopropyl alcohol pad and erse the cable in any liquid solution. Do not

7-5



leaning (continued)

O2 Cleaning ocedure

To clean the SpO2 sensor, disconnecLNOP DCI by wiping it with a 70% isobefore placing back in use.Clean the patient cable by wiping it wallowing it to dry. Do not soak or immattempt to sterilize.



C

InPr capacitor carries high voltage. Remove

citor before handling.

n any part of this device or accessories enolic compounds. Do not use abrasive ot attempt to sterilize this device or any

cified in accessory operating

scribed below. with a nonmetallic, soft-bristle brush.sing a dry, low-pressure compressed air

onabrasive cloth that has been dampened

7-6



leaning (continued)

ternal Cleaning ocedure

WARNING!Shock hazard. The energy storagethe battery and discharge the capa

CAUTION!Possible case damage. Do not cleawith bleach, bleach dilution, or phor flammable cleaning agents. Do naccessories unless otherwise speinstructions.

Clean the interior of the device as de1. Brush interior surfaces and parts2. Remove loosened dirt and dust u

(60 psi) or vacuum cleaner.3. Wipe metal surfaces with a soft, n

with isopropyl alcohol.



D

ice and subassemblies are subjected to the routine testing and maintenance e manual will help provide reliable device

anges and the availability of replacement medical devices. The American Hospital ful life expectancy for defibrillators le Hospital Assets, Revised 1998 Edition). -year life expectancy for defibrillators nditure Limits for Medical Materiel, TB

Su support and replacement parts for a period nt from our manufacturing facility. After this vides technical support and replacement

7-7



evice Useful Life

During product development, the devrigorous life testing. This testing and program recommended in this servicoperation for many years.However, both rapid technological chparts limit the useful life of all modernAssociation suggests a five-year use(Estimated Useful Lives of DepreciabSimilarly, the U.S. Army lists an eight(technical bulletin: Maintenance ExpeMED 7 Revision 8 October 1993).

pport Policy Physio-Control provides full technicalof eight years from the date of shipmeeight-year period, Physio-Control proparts on an as-available basis.



S

ds of storage, connect the device to ac rge the batteries at an ambient room ° F), prior to storage and before use.e without turning off the AC Loss Alert

AC that beeps when the device is turned off urce. The alarm can be configured to beep t can be turned off. The default setting is

menu. ETUP/GENERAL submenu. MINUTES, or NEVER ALERT to set or turn off

7-8



toring the Device

When not in use, or during long periopower. If this is not possible, fully chatemperature, not to exceed 25° C (77Note: Do not store or ship the devic

alarm.

Loss Alert Alarm The device is equipped with an alarmand not connected to an ac power soat 5-, 15-, or 30-minute intervals, or i15 minutes.To set or disable the alarm:1. Display the SETUP menu. 2. Select GENERAL from the SETUP 3. Select AC LOSS ALERT from the S4. Select 5 MINUTES, 15 MINUTES, 30

the alarm.



R

seful life. the device according to national and local ysio-Control representative for assistance

com/recycling. be clean and contaminant-free prior to

— After using disposable electrodes, follow recycling.iscarding/Recycling Batteries.ckaging materials.

7-9



ecycling

Recycle the device at the end of its u■ Recycling assistance — Recycle

regulations. Contact your local Phor refer to www.physio-control.

■ Preparation — The device shouldbeing recycled.

■ Recycling disposable electrodes your local clinical procedures for

■ Recycling batteries — Refer to D■ Packaging — Save or recycle pa




BM

is section to help maximize battery life and

ry

ries



10attery aintenance

Follow the guidelines described in thperformance.

Types of BatteriesCharging the Backup BatteStoring the BatteryDiscarding/Recycling Batte


LIF Battery Maintenance

Ty

or the device. in the bottom case. itor uses a 10-cell, nickel metal hydride

nitor uses a 9-cell, lithium-ion (Li-ion)

itor battery will not be charged or may other than a Physio-Control battery is

d as the primary power source. If the e to power outage or other reason, the for at least two hours.ry that delivers a continuous flow of power ories. This battery has a greater than five-nd should be replaced at the end of its life.

8-2



pes of Batteries

AC power is the main power source fThere is one backup battery located ■ The LIFEPAK 20 defibrillator/mon

(NiMH) battery.■ The LIFEPAK 20e defibrillator/mo

battery.

WARNING!The LIFEPAK 20e defibrillator/monbe charged incorrectly if a battery used.

This battery is not intended to be useprimary power source is removed, dubackup battery will power the device The device also has a coin cell batteto the internal clock and other accessyear life span. It is not rechargeable a



C

has a built-in, high-current charger that ackup battery in approximately two hours evice. The charger does not recharge the nce the battery’s last full recharge or until nd then reconnected.r has a built-in, constant, current-constant pletely discharged backup battery in wer is connected to the device. The y until the Li-ion battery's state-of-charge

r/monitor will only initiate battery charging if C. If extensive defibrillator shocks have high ambient temperature, the battery will g.

8-3



harging the Backup Battery

The LIFEPAK 20 defibrillator/monitorrecharges a completely discharged bwhen ac power is connected to the dbattery until one week has passed sithe battery has been disconnected aThe LIFEPAK 20e defibrillator/monitovoltage charger that recharges a comapproximately four hours when ac pocharger does not recharge the batterdrops below 85%. Note: The LIFEPAK 20e defibrillato

the battery pack is below 40°been applied to a device in anot immediately start chargin



S

in storage when it is not in active use.andling procedures for storage. Store the 0° C (-4° F and 122° F). Lower tial charge.

8-4



toring the Battery

A battery packet is considered to be The battery packet requires special hbattery packet between -20° C and 5temperatures reduce the battery’s ini



D

at end of its useful life if one or more of the

battery.

ss of full charge capacity.al and local regulations. Contact assistance at 1.800.442.1142, or refer to for disposal instructions.

Do not recharge, disassemble, crush, te, or mistreat batteries.

8-5



iscarding/Recycling Batteries

A battery should be considered to befollowing circumstances occur:■ There is physical damage to the ■ The battery is leaking.■ The battery charges to 80% or leRecycle batteries according to nationPhysio-Control Technical Support forwww.physio-control.com/recycling

WARNING!Risk of fire, explosion, and burns. heat above 100°C (212°F), incinera




RP

f detailed instructions for disassembly, ble LIFEPAK 20/20e defibrillator/monitor

ever the device case is opened for service. harnesses, label the cables and y during reassembly (for example, J1, J3, for additional information.

es, item numbers in parentheses refer to Parts List.

rge Toolation




11eplacement rocedures

Replacement procedures are a set ohandling, and reassembly of replaceaassemblies.Perform an interior inspection whenWhen disconnecting cables and wireconnections so that they match easiletc.). See the Interconnect DiagramNote: Within replacement procedur

parts that are in the section’s

Repair Procedures IndexWarnings and CautionsRoHS StandardsCapacitor Discharge ToolUsing the Capacitor DischaSaving the Setup ConfigurMain Assemblies



RP(c

entrial Number



eplacement rocedures ontinued)

Interconnect DiagramBattery ReplacementTop CaseFront CaseBoardstackBottom CaseFinal AssemblyService Replacement KitsDevice Software ReplacemDevice Part Number and SeOrdering Parts


LIF Replacement Procedures

RCh n device disassembly order from left to rigB

ToP Top Case Installation


FA Parts ListF Front Case RemovalF AED Door ReplacementW A15 Elastomer Keypad RemovalA A11 Active Display InstallationA W17 Backlight Inverter Cable DiagramsA n A05 User Interface PCB DiagramW W04 Speed Dial Assembly InstallationW W04 Speed Dial Assembly DiagramsW

9-3



epair Procedures Indexoose from the following replacement procedures (procedures are listed iht):attery Replacement

p Casearts List Top Case Removal

ront Casessembly Diagram (Front View) Assembly Diagram (Rear View)ront Case Disassembly Front Case Reassemblyront Case Installation Grounding Harness Orientation18 UI Flex Cable Removal W18 UI Flex Cable Installation15 Elastomer Keypad Installation A11 Active Display Removal08 Backlight Inverter PCB Diagram A11 Active Display Diagram05 User Interface (UI) PCB Removal A05 User Interface (UI) PCB Installatio18 UI Flex Cable Diagrams W04 Speed Dial Assembly Removal02 Speaker Assembly Removal W02 Speaker Assembly Installation02 Speaker Assembly and W25 Speaker Harness Extension Cable Diagrams



R


BA Parts ListB Boardstack Removal

B W07 Capacitor Discharge Cable Diagram

A A10 SpO2 Module Installation

A A02 Patient Parameter and A06 OEM/SpO2 Assembly Installation

A A01 System PCB RemovalA A04 Therapy PCB Removal

A g) A04 Therapy PCB Diagram (Without Pacing)

9-4



epair Procedures Index (continued)

oardstackssembly Diagram A04 Therapy PCB Assembly Diagramoardstack Disassembly Boardstack Reassembly

oardstack Installation W07 Capacitor Discharge Cable Replacement

14 Inductive Resistor Diagram A10 SpO2 Module Removal

10 SpO2 Module Diagram A02 Patient Parameter and A06 OEM/SpO2 Assembly Removal

02 Patient Parameter PCB Diagram Coin Cell Battery Replacement01 System PCB Installation A01 System PCB Diagram

04 Therapy PCB Installation A04 Therapy PCB Diagram (With Pacin



R


BA Parts List B A12 Printer Module RemovalA A13 Energy Capacitor RemovalA A03 Power Module InstallationA s W06 ECG Connector RemovalW ms W01 Therapy Connector Removal

W W01 Therapy Connector Assembly Wiring Diagram

W W05 SpO2 Assembly DiagramsW W03 IrDA Assembly DiagramsW

9-5




ottom Casessembly Diagram (Modules) Assembly Diagram (Connectors)ottom Case Disassembly Bottom Case Reassembly12 Printer Module Installation W14 Printer Flex Cable Diagrams13 Energy Capacitor Installation A03 Power Module Removal03 Power Module Diagram W11 ECG Sync/System Cables Diagram06 ECG Connector Installation W06 ECG Connector Assembly Diagra

01 Therapy Connector Installation W01 Therapy Connector Assembly Diagrams

05 SpO2 Connector Removal W05 SpO2 Connector Installation03 IrDA Assembly Removal W03 IrDA Assembly Installation25 Speaker Harness Extension Cable

RemovalW25 Speaker Harness Extension CableInstallation



R

FD

Manual Latch Label Languages

A A15 Elastomer Keypad - LanguagesIS Charge Button Languages

9-6




inal Assemblyevice Labeling Including Label Set (12) 3201640 - LIFEPAK 20 3206034 - LIFEPAK 20e

LIFEPAK 20/20e Device Label Set Languages

ED Door/Latch Label Kits A15 Elastomer Keypad – All Optionsnstalling Printer Paper Standard Paddles Labels and Buttonstandard Paddles Parts List Standard Paddles Label Languages



W

utions apply to all actions you may ice.

e must be performed by properly trained ntially lethal charges accessible inside the the procedures carefully for discharging the

oltage. Discharge the capacitor before

during reassembly. To avoid pinching wires, .

PCB assemblies contain static-sensitive bserve the special handling practices vices (SSD).

9-7



arnings and Cautions

The following general warnings and caperform during maintenance of the dev

WARNINGSHOCK HAZARD. Servicing of this devicindividuals. This device may retain potedevice at any time, even when off. FollowA13 Energy Capacitor.

The A13 Energy Capacitor carries high vhandling.

It is possible to pinch and damage wirescarefully follow reassembly instructions

CAUTIONPossible component damage. Thedevices (SSDs). To avoid damage, odescribed under Static-Sensitive De



R

Ab w directive which applies to all medical s 2011/65/EU of the European ly referred to as “RoHS 2” (Restriction of

requires companies to restrict the use of ir products (such as lead, mercury, etc.).0e device have been updated to comply h RoHS-certified and non-RoHS parts

rts are functionally equivalent. However, the following RoHS vs Non-RoHS Parts rts to order. 20e devices that are RoHS compliant can ber label. The product part number for a number of 300 or greater.

9-8



oHS Standards

out RoHS Parts The European Union has initiated a nedevices sold in Europe. This directive iParliament and the Council, commonHazardous Substances). The directivecertain substances in the design of theSome of the parts in the LIFEPAK 20/2with this standard. For these parts, botmay be listed. RoHS-certified parts and non-RoHS pawhen ordering parts replacement, use Replacement Rules to decide what paRoHS Device Identification—LIFEPAKbe identified by the product serial numRoHS version is 3202488 with a dash



R

Ab(c

lesNon-RoHS Country (ROW)

IR

RoHS or non-RoHS equivalent parts can be used to service any device

IL

RoHS or non-RoHS equivalent parts can be used to service any device

RL

It is OK to put a non-RoHS accessory on a RoHS device. Existing inventory will be depleted and replaced by RoHS compliant accessories

9-9



oHS Standards (continued)

out RoHS Parts ontinued)

RuSituation RoHS Country (Europe)

f replacing parts in a LP20e oHS device

ALL parts must be RoHS

f replacing parts in a LP20e or P20 non-RoHS device

RoHS or non-RoHS equivalent parts can be used until inventory is exhausted

eplacing accessories on a P20e or LP20 device

It is OK to put a non-RoHS accessory on a RoHS device. Existing inventory will be depleted and replaced by RoHS compliant accessories



S

Ab s (such as MOS ICs, FETs, optical aged by the discharge of static electricity. Static discharges commonly occur when nd transfers the charge to any object e or destroy static-sensitive devices s not even perceptible to the person who

SSDs, observe the following precautions e, or repair procedures:

Th arning symbol:

on a static-dissipative mat that is


9-10



tatic-Sensitive Devices (SSD)

out SSD Handling Many electronic semiconductor deviceisolators, or film resistors) can be damStatic-charge buildup is very common.the operator wears synthetic clothes atouched. These discharges can damag(SSDs). In most cases, the discharge icauses it.To prevent static-discharge damage toduring any open-case test, maintenanc

e SSD Symbol SSDs are identified with the following w

Always perform repair or maintenanceconnected to earth ground.

ATTENTION



S

W ap connected to the mat and to ground equipment or when discharging high snug enough to make good contact

TrPC

racks or inside conductive bags. Label static-sensitive.

KeSt

as styrofoam cups or trays, away from the ment, such as test equipment, to ground

TeRo

(mat, straps, cables) routinely. Keep a

trap when working on energized equipment or ts.

9-11



tatic-Sensitive Devices (continued)

ear a Wrist Strap • Always wear a conductive wrist strexcept when working on energizedvoltage circuits. The strap must beagainst bare skin.

ansport and Store Bs Properly

Transport and store PCBs in anti-staticthe package that contains the PCBs as

ep Work Area atic-Free

Keep static-generating products, such work area. Connect all electrical equipwith a three-prong plug.

st Work Area utinely

Test all antistatic parts of the work arealog of the test results.

WARNINGSHOCK HAZARD. Remove the wrist swhen discharging high-voltage circui



A

To PAK 20/20e defibrillator/monitor

pags

on about Capacitor Discharge Tool)rque settings are 6.8 and 10.0 in-lb.

s tip for 4-40 screws (shaft length of 2”)s tip for 6-32 screws (shaft length of 2”)

Values10.0

160

113

9-12



ssembly Tools List

ols List The suggested list of tools for the LIFEreplacement procedures is as follows:■ Static-dissipative mat and wrist stra■ Anti-static rack and/or conductive b■ Capacitor discharge tool (informati■ Torque screwdriver(s) - required to

■ Point 1 power drive bit (P1)- Phillip■ Point 2 power drive bit (P2)- Phillip■ 3/32” Allen Driver■ 1/4” Nut Driver

Torque MeasurementsTorque in-lb 6.8

Torque in-oz 108.8

Torque cNm 77



C

e tools are available. Contact a Technical ation.

sic capacitor discharge tool is constructed e Capacitor. The materials used in this

, high-voltage

ulating 10 kV

rgy storage capacitor, continue to the

t are not designed and labeled for biphasic c defibrillators. They will take several minutes

5r

9-13



apacitor Discharge Tool.

Third party biphasic capacitor dischargSupport Representative for more informShown is an example of how the biphafor discharging the A13 Energy Storagexample are:■ 10 k, 2 W resistor (ten 1 K 2 W)■ 5 M, 5 W resistor, high-voltage■ Neon lamp, NE76, NE2, or NE2H■ 8 AWG copper wire■ Clear plastic tubing, capable of ins■ 10 kV insulation■ RTV, silicone rubber sealantFor instructions on discharging the enenext page.

WARNINGSHOCK HAZARD. Discharge tools thause are inadequate for use on biphasito discharge the energy capacitor.

RTV silicone rubber sealant

10K 2W resistor

RTV silicone rubber sealant

10 kV insulation

8AWG wire

Neon lamp

M5W esistor

Clear plastic tubing

6 inches



U

discharge the energy storage capacitor the inner parts of the device.

t on the inductive resistor and hold it ext page).tion point of the capacitor wire. Hold both

capacitor discharge tool. If a charge of the neon lamp will light.

t are not designed and labeled for biphasic c defibrillators. They will take several minutes


9-14



sing the Capacitor Discharge Tool.

The capacitor discharge tool is used tobefore beginning any maintenance on To use the capacitor discharge tool:1. Remove the battery. 2. Remove the top case.3. Place one probe on the solder join

steady (see the illustration on the n4. Place the other probe in the connec

probes steady.5. Observe the neon lamp inside the

approximately 90 volts is present,

WARNINGSHOCK HAZARD. Discharge tools thause are inadequate for use on biphasito discharge the energy capacitor.



U )

e points indicated for at least 30 seconds .

capacitor is discharged if the neon lamp does on the capacitor. Do not touch capacitor rge operation.

Pin 5 on the A04 Therapy PCB P2 connector. See the Interconnect Diagram for more detail.

9-15



sing the Capacitor Discharge Tool (continued.

6. Continue holding the probes on thafter the neon lamp is no longer lit

WARNINGSHOCK HAZARD. Do not assume thenot light! There may still be a chargeterminals until completing the discha

Solder point on inductive resistor

Capacitor discharge cable connection point

Capacitor discharge cable passes under the W01 Therapy Cable and wraps around the J13 connector.Position the therapy cable ferrites so that they will not damage the J13 connector



to save the device setup configuration

System account, then use the LIFENET e setup configurations.etup configuration to a spare device, r the setup configuration back again. p configuration, complete repairs, and

ce.nsferring it to a spare device requires that ftware version. Otherwise, potentially when the configuration is restored to the yright dates are the same on the es.

9-16


LIFEPAK 20/20e Defibrillator/Monitor Saving the Setup Configuration

The following procedures describe howbefore beginning any repair action. ■ If the device owner has a LIFENET

Device Agent application to manag■ Another method is to transfer the s

complete repairs, and then transfe■ The final method is to print the setu

then manually reconfigure the deviNote: Saving the configuration by tra

both devices have the same sounexpected results may occur repaired device. Verify that copintroduction page of both devic



spare device:es, connect the two devices using a 202447) between the device system

evices.menu on the device to be repaired. The

DIAL. The setup configuration transfers to

P menu on the device to be repaired. The figuration. Save this backup printout for

ransferring it back to the repaired device: saved setup configuration) to the

ion transfer cable (P/N 3202447) between


9-17


LIFEPAK 20/20e Defibrillator/Monitor Saving the Setup Configuration (continued)

Transferring the Setup Configuration

To transfer the setup configuration to a1. With the power OFF on both devic

configuration transfer cable (P/N 3connectors.

2. Display the SETUP menu on both d3. Select SEND CONFIG in the SETUP

SEND CONFIG overlay appears. 4. Select SEND and press the SPEED

the spare device.5. Select PRINT DEFAULTS in the SETU

printer prints the device setup conpossible future reference.

6. Turn both devices OFF.

Restoring the Setup Configuration

To restore the setup configuration by t1. Connect the spare device (with the

repaired device using a configuratthe device system connectors.



evices.enu on the spare device. The SEND

DIAL. The setup configuration transfers

r prints the device setup configuration. ce.

e SETUP menu.gs in each menu and revise as necessary

9-18


LIFEPAK 20/20e Defibrillator/Monitor Saving the Setup Configuration (continued)

2. Display the SETUP menu on both d3. Click SEND CONFIG in the SETUP m

CONFIG overlay appears.4. Select SEND and press the SPEED

back to the repaired device.5. Turn both devices OFF.

Printing the Setup Configuration

To print the setup configuration:1. Display the SETUP menu.2. Select PRINT DEFAULTS. The printe

Save this printout for future referen3. Turn the device OFF.4. Make the necessary repairs.5. Turn the device ON and display th6. Using the printout, check the settin

to match the printout. 7. Turn the device OFF.



M

Printer Module

Power Module

Fr

9-19



ain Assemblies

Interconnect

Top Case Assembly

Boardstack Assembly

Bottom Case Assembly

ont Case Assembly



In

A08 Backlight Inverter PCB

Power Module

A12 Printer

A11 LCD Display PCB

W09 W10LP20e

W11

W14W01

W23 W24

W22W21W20

W15

W17

W19

A05 User Interface PCB

J37 J36 J34P34P37

P14J14

P13J13

J17P17P16

J16

J45

J47 P47

P45

P41 P51

P70

P74PCB Shield

Display Bracket

Printer Shroud

J81 TherapyPower BracketHeatsink

PCB Bracket

J48RS-232

J49Sync inECG out

J2

CN101

J39 Test

J38 Test

J1

J51J41

9-20



terconnect Diagram

A10 SpO2 PCB

A06 OEM PCB

A02 Patient Parameter PCB

A01 System PCB

A04 Therapy PCB

A19 EMI Line Filter

A03

A13 Energy Capacitor A14 Inductor/Resistor

W08LP20e

W18 UI FlexW06

W03 W25 W02

W12

W04W05

A09 AC Power Supply

A07 Battery

J03

J52J01J53

P24

J24

J54 P54

J32P32 J31

P23J23 J21 J22

P31

P21

J01 J02

J02J01

J11 J12J01P01P02

J02J15

J03

J08P08 P05

J05

P06 P07IrDA

P03

ECG 8-Pin Conn.

J21 J22

J50P50

P85J85

J01 P61

P62J02

J46 AC Power

P49

Cap Discharge

J80Gnd Stud

W13LP20e

Speaker

J83 SpO2

Speed Dial J82 ECG

J33 Test

W07

J49

P


9-21Ba

A0Re

r the A07 Batteries. The LIFEPAK 20e

PAK

tery

Batt


07 Battery with the 6-pin connector, and nitor uses the battery with the 4-pin

Battery from the device:er.

drivers into the door taps and pinch the 3).attery.

the A07 Battery.ery compartment. (For the LIFEPAK 20 ward the rear of the device.) compartment with the wire harness

e.

PIP.

Main Assemblies


E 20/20e Defibrillator/Monitor

t Replacement

7 ery placement

Note: There are two different types fodefibrillator/monitor uses the Athe LIFEPAK 20 defibrillator/moconnector. To remove the A07

1. Disconnect the device from ac pow2. Place the device top down.3. Insert two, small, flat-bladed screw

tabs to remove the battery door (104. Remove and disconnect the A07 BTo install the A07 Battery:1. Place the device top down.2. Connect the W08 Battery Cable to3. Insert the A07 Battery into the batt

battery, ensure the fuse is facing toNote: Install the A07 Battery in thefacing toward the front of the devic

4. Close the battery door (103).5. Complete the LIFEPAK 20 Device

103A07Battery

Parts List Modules View



To

Toer.

e device.

0.375 screws (169) securing the bottom

75 screws (167) securing the bottom case

1.75 screws (167) securing the top case ).m the top case, and slide the top case up ce.

ain Assemblies

9-22



p Case

p Case Removal To remove the top case:1. Disconnect the device from ac pow2. Remove the A07 Battery from th3. Place the device face down.4. Remove and discard the two 6-32

case to the front case.5. Remove and discard the 6-32 1.

to the top case.6. Place the device on its bottom.7. Remove and discard the two 6-32

to the front case (outboard screws8. Pull the front case slightly away fro

and away from the rest of the devi9. Discharge the A13 Capacitor.

169

167

167

Parts List M



To

Tocase.tom case..

se with two new 6-32 1.75 screws (167);

ure the front case to the bottom case with ); torque to 10 in-lb.m case with two new 6-32 1.75 screws

vice.nstall new labels. PIP.

24

Main Assemblies

9-23



p Case (continued)

p Case Installation To install the top case:1. Align the front case to the bottom 2. Align the top case (242) to the bot3. Align the front case to the top case4. Secure the top case to the front ca

torque to 10 in-lb.5. Turn the device face down and sec

two new 6-32 0.375 screws (1696. Secure the top case onto the botto

(167); torque to 10 in-lb.7. Install the A07 Battery into the de8. Review the labels parts list and i9. Complete the LIFEPAK 20 Device

169

167

167

2

Parts List



To

Pa

It tion Note

1 ws 6-32 × 1.75L

1 w, 6-32 × 0.375L

2 embly

9-24



p Case (continued)

rts List

em Quantity MIN CAT. Part Descrip

67 4 202253-592 21300-005334 Machine scre

69 2 202253-570 21300-001032 Machine scre

42 1 3202497-002 21330-001036 Top case ass



F

As(F

Rear View Main Assemblies

A15

37

199

23

19

without door optionFrFrA(1WRWInARAIn

9-25



ront Case

sembly Diagram ront View)

Parts A05–W18 Parts 9–47 Parts 161–284

912-D

W04

17

12-B12-C

Hardware suppliedwith item W04

ont Case Removal (9)ont Case Installation (9)ED Door Replacement 99)04 Speed Dial Assembly emoval 04 Speed Dial Assembly stallation15 Elastomer Keypad emoval15 Elastomer Keypad stallation

12-Bno SpO2

w/ SpO2

284



F

As(R

Pa ront Case View Main Assemblies

Detail A

9 Ref 201 only used

A1A1A0ReA0InWWInGr

41 W04

9

A05

173 (x4)

161 (x3)see Detail A

221

240

219 250W02

(x2)

with A08- 3202033

9-26



ront Case (continued)

sembly Diagramear View)

rts A05–W18 Parts 9–47 Parts 161–284 F

A08

47

A11

43

266

173 (x4)

219 (x2)

1 Active Display Removal1 Active Display Installation5 User Interface (UI) PCB moval5 User Interface (UI) PCB

stallation02 Speaker Assembly Removal02 Speaker Assembly stallationounding Harness Orientation

173(x2)

3308907



F

Pa


Pa Rear View Main Assemblies

Ite NoteA0 Part of kit MIN 3202718-044,

3202718-045, 3202718-046A0 T,

V inPart used with A11 - 3205278 Part of kit MIN 3202718-009

A0 ver Part used with A11 - 3309555 Part of kit MIN 3202718-032

A1 CD Part of kit MIN 3202718-008A1 ED Requires A05 - 3317230-002 or

greater and Redux Device S/WPart of kit MIN 3202718-032

A1 Select other language

9-27




rts List

rts W17–47 Parts 161–284 Front Case View

m Quantity MIN CAT. Part Description5 1 3317230-002 see note User Interface PCB

8 1 3202033 see note Backlight Inverter, CCFLCD, 1.5KV Out, 8to20

8 1 3308907 see note Module-OEM, LED Dri(Backlight Inverter)

1 1 3205278 see note Active Display, Color L

1 1 3309555 see note Active Display, Color L

5 1 3200642-XXX see note Elastomer Keypad



F

Pa



It Note

W RoHS

W Non-RoHS

W

W able

W er Cable

W bly

9 Part of kit MIN 3202718-001

12 Refer to Labels Assembly

17


23 Select other language

9-28




rts List (continued)

Parts A05–W15 Parts 161–284 Front Case View

em Quantity MIN CAT. Part Description

02 1 3319086-001 21300-008133 Speaker Assembly

02 1 3201593-004 21300-004247 Speaker Assembly

04 1 3201145-000 21300-004264 Speed Dial Assembly

15 1 3300152-000 21300-007774 Active Color Display C

17 1 3200996-002 21300-004237 Active Backlight Invert

18 1 3201000-004 21330-008056 UI to Stack Flex Assem

1 3200624 see note Front case

1 3206034-XXX see note Label set (6 labels)

1 3200633-000 21300-004620 Speed Dial knob

1 3200638-001 21300-004837 Cover plate, door

1 3201499-009 21501-000767 Manual latch label



F

Pa

P Rear View Main Assemblies

Ite Note


41 ting

43 Part of various kits


16

17 0.312L

19 Part of kit MIN 3202360

20 acklight

21 ss Active Display

22 ss User Interface PCB

9-29






arts A05–W15 Parts W17–47 Front Case View

m Quantity MIN CAT. Part Description

1 3200637-001 21300-004836 Door hinge plate

1 3201610-000 21300-004649 Bracket, speaker moun

1 3200913-003 21300-004233 Display lens

1 3200640-015 21300-004838 Active display bracket

1 3 200805-000 21300-000584 Locking hex nut, 4-40

3 10 202253-761 21300-001038 Machine screw, 4-40

9 1 3202056-XXX see note AED door assembly

1 1 3201111-003 21300-004241 Thermally conductive binverter pad

9 3 3202246-003 21300-004254 Grounding strap harne

1 2 3202246-004 21300-004255 Grounding strap harne



F

Pa

Ite Note


25 ss,

26 Part of various display kits

28 Refer to labels assembly

9-30







0 1 804447-041 21300-004807 Spacer Foam, UI PCB

0 1 3202246-005 21300-004884 Grounding strap harneSpeed Dial

6 1 3205497-308 21300-006141 Nylon snap rivet

4 1 3206926-XXX see note Label - Adult VF Dose

Parts List Interconnect Front Case View



F

FrDi evice.

ice is equipped with a door).

CB.embly.bly.ue to Front Case Reassembly.

ear View Main Assemblies

9-31




ont Case sassembly

To disassemble the front case:1. Remove the front case from the d2. Remove the AED door (if the dev3. Remove the A11 Active Display.4. Remove the A05 User Interface P5. Remove the W04 Speed Dial Ass6. Remove the W02 Speaker Assem7. Replace the front case and contin

Interconnect Front Case View R



F

FrRe ly.

B. bly.

d. is equipped with a door).

stall new labels.PIP.

ar View Main Assemblies

9-32




ont Case assembly

To reassemble the front case:1. Install the W02 Speaker Assemb2. Install the A05 User Interface PC3. Install the W04 Speed Dial Assem4. Install the A11 Active Display. 5. Install the A15 Elastomer Keypa6. Install the AED door (if the device7. Install the front case.8. Install the top case.9. Install the A07 Battery.10. Review the labels parts list and in11. Complete the LIFEPAK 20 Device

Interconnect Front Case View Re



F

Fr

citor.esses (219) that connect the A11 Active ort bracket by removing and discarding

ed grounding straps.oardstack assembly and disconnect the atient Parameter (PP) PCB at J21 and

assembly instructions to avoid a shock or



9-33




ont Case Removal

To disassemble the front case:1. Remove the A07 Battery.2. Remove the top case.3. Discharge the A13 Energy Capa4. Disconnect the two grounding harn

Display to the top of the PCB suppthe two screws (173).Note: Replace any broken or fray

5. Pull the front case away from the bW18 UI Flex Cable from the A02 PJ22.

W18219

221

219

(x2)

173 WARNINGSHOCK HAZARD. Carefully follow disdamage to wires during disassembly.




F

Fr(c

esses (221) that connect the bottom left nterface (UI) PCB to the PCB support g the two screws (173). (219) that connects the bottom center of rt bracket by removing and discarding the

ess Extension Cable from the W02

able from the A05 UI PCB at J34.connector to access the printer connector.evice.


9-34




ont Case Removal ontinued)

6. Disconnect the two grounding harnand right corners of the A05 User Ibracket by removing and discardin

7. Disconnect the grounding harnessthe A05 UI PCB to the PCB supposcrew (173).

8. Disconnect the W25 Speaker HarnSpeaker Assembly.

9. Disconnect the W14 Printer Flex CNote: Disconnect the Speed Dial

10. Pull the front case away from the d




FFr

le to the A05 UI PCB at J34.s Extension Cable to the W02 Speaker

le if it was disconnected during the

s (221) by connecting the bottom left and the PCB support bracket, using two new efer to Grounding Harness Orientation

) by connecting the bottom center of the tem shield, using a new screw (173);

grounding harnesses must be installed at vice components.



9-35




ont Case Installation To install the front case assembly:1. Connect the W14 Printer Flex Cab2. Connect the W25 Speaker Harnes

Assembly.Note: Reconnect the SPEED DIAL cab

disassembly process.

3. Install the two grounding harnesseright corners of the A05 UI PCB toscrews (173); torque to 6.8 in-lb. Rfor grounding harness placement.

4. Install the grounding harness (219A05 UI PCB to the boardstack systorque to 6.8 in-lb.

W18219

221

219

(x2)

173

CAUTIONPossible component damage. Theprecise angles to avoid damaging de

arts List Interconnect Front Case View



F

Fr(c

the A05 UI PCB at J36.tor Lock on the A02 PP PCB.r the latch on the A02 PP PCB at CN101 the latch. ses (219) by connecting the top of the ng two new screws (173); torque to 6.8 in-rientation for grounding harness

y


9-36




ont Case Installation ontinued)

5. Connect the W18 UI Flex Cable to6. Unlatch the Display CN101 connec7. Install the W18 UI Flex Cable unde

connector until seated, then close 8. Connect the two grounding harnes

front case to the system shield, usilb. Refer to Grounding Harness Oplacement.

9. Return to Front Case Reassembl




F

GrOr

, and bottom case join correctly, align the and on the next page.



B

C

E

D

9-37




ounding Harness ientation

To ensure that the top case, front casegrounding harnesses as shown below


A

AB

CD

E



F

GrOr

Grounding Harness lug orientation

Active Display removed for clarity


9-38




ounding Harness ientation (continued)

219

221

Grounding Harness lug orientation219




F

AERe

be an easily replaceable, breakaway ntly comes off during use, follow step 3 of low.bly:

hinge pin center slightly away from the free of the hinge.

adhesive.

he door hinge plate (37) to the front case. hinge pin center slightly away from the into the hinge. Ensure that the hinge pins


9-39




D Door placement

The AED door assembly is designed toassembly. If the door assembly accidethe AED door installation procedure beTo remove the entire AED door assem1. Open the AED door.2. Use a small screwdriver to pry the

door assembly until the door slides3. Peel the hinge off the front case.4. Clean the front case to remove old

To install a new AED door assembly:1. Clean the hinge area.2. Expose the adhesive and secure t3. Use a small screwdriver to pry the

door assembly until the door slidessnap into the securing holes.




F

WRe

d before beginning this disassembly.

t the two grounding straps (219) that the system shield, by removing the two

n the grounding harnesses. If they are , the front case will not join with the rest of

away from the boardstack assembly, and from the A02 PP PCB at J21 and J22. from the A05 UI PCB at J31, and remove


9-40




18 UI Flex Cable moval

Note: The top case must be removeTo remove the W18 UI Flex Cable:1. From the system shield, disconnec

connect the top of the front case toscrews.Note: Observe the positioning onot reinstalled at the correct anglesthe device correctly.

2. Pull the front case slightly forward,disconnect the W18 UI Flex Cable

3. Disconnect the W18 UI Flex Cablethe cable from the device.




F

WIn orward and away from the boardstack

x Cable to the A05 UI PCB at J31.lex Cable during installation. Excessive

nnectors.Cable to the A02 PP PCB at J21 and J22, the connectors evenly to avoid possible

(219) by connecting the top of the front e two screws (173); torque to 6.8 in-lb.f the grounding harnesses. If they are , the front case will not join with the rest of


9-41




18 UI Flex Cable stallation

To install the W18 UI Flex Cable:1. With the front case pulled slightly f

assembly, connect the W18 UI FleNote: Avoid bending the W18 UI Fbending can damage wires and co

2. Carefully connect the W18 UI Flex ensuring that the pins connect withpin damage.

3. Connect the two grounding straps case to the system shield, using thNote: Observe the positioning onot reinstalled at the correct anglesthe device correctly.

4. Reassemble the top case.




F

A1Re

: front case.

A1In configurations to find the MIN (part

your device:

case, position the left and right bottom d flush against the bottom corners of the

nto the front case ensuring that it is flush s or gaps.


9-42




5 Elastomer Keypad moval

To remove the A15 Elastomer Keypad1. Peel the old keypad away from the2. Thoroughly clean the front case.

5 Elastomer Keypad stallation

To install the A15 Elastomer Keypad:1. Select one of the following device

number) for the correct keypad for– Keypad View– Keypad Parts List

2. After thoroughly cleaning the front edges of the A15 Elastomer Keypafront case.

3. Press the A15 Elastomer Keypad oagainst the case with no air pocket




F

A1Re

lies before beginning this disassembly:

Cable (see illustration) from the

cking tab away from the connector.t (leave the cable connected to the UI

rter Cable from the A05 UI PCB at J37. 0.312 screws (173) from the display

g harnesses (219) attached to the top . Replace any broken or frayed grounding

bly from the front case. A



9-43




1 Active Display moval

Note: Remove the following assemb– Top case– Front case

To remove the A11 Active Display:1. Disconnect the W15 Active Display

A11 Active Display, as follows:– Gently pull both sides of the lo– Pull the cable out of the socke

PCB).

2. Disconnect the W17 Backlight Inve3. Remove and discard the four 4-40

assembly cover.Note: Remove the two groundintwo screws of the display assemblyharnesses.

4. Remove the display bracket assemW15

(connects to A05)11

W17

A08

47

173

219

(x4)

(x2)




F

A1Re

parts. Remove and replace any part that ged connectors.ove, disconnect the Active Display wires ht Inverter Cable at J1. Pull the backlight ket. A new display bracket is required e pre-attached.

remove, disconnect it from the A05 UI disconnected from the Active Display in

To remove, disconnect it from the A05 UI A08 Backlight Inverter (if not previously d out of the molded notches on the

oving above parts, replace if necessary. ght Inverter PCB adhesive and the Active

(used only with 3202033 - A08 Backlight old pad located on the top inside edge of

ill


9-44




1 Active Display moval (continued)

5. Check the condition of the followinghas cracks, broken wires, or damaA08 Backlight Inverter — To remat J2. Disconnect the W17 Backliginverter away from the display bracbecause the adhesive and foam arW15 Active Display Cable — To PCB at J36 (cable was previously step 1).W17 Backlight Inverter Cable —PCB at J37. Disconnect it from theremoved) at J1. Pull the ferrite beadisplay bracket.Display bracket (47) — After remThe display bracket has the BackliDisplay foam pre-attached.Thermal conductive pad (201) —Inverter) To remove, peel away thethe top case (see illustration 2).

W17

47

A08

Align to right edge of bracket flange

ustration 1




F

A1In parts and replace if necessary:

stration 1) illustration 3)see illustration 1)tration 1) located on the top inside edge of the top

is only required when using A08 The thermal conductive pad must be ter edge of the front case (past the ends of case)d (201), if necessary, by peeling away the dhesive, and applying the new pad to the centered between the locator notches.

o

illu

OIn



9-45




1 Active Display stallation

To install the A11 Active Display:1. Verify the condition of the following

– A08 Backlight Inverter (see illu– W15 Active Display Cable (see– W17 Backlight Inverter Cable (– Display bracket (47) (see illus– Thermal conductive pad (201),

case.Note: The thermal conductive pad

Backlight Inverter - 3202033.positioned flush against the outhe locator notches in the front

2. Replace the thermal conductive paold pad, removing any remaining aupper inside edge of the top case,

bottom edge

bottom edge

201

outer edge

uter edge

stration 2

nly required with Backlight verter - 3202033




F

A1In

ter, a new display bracket (47) is required. ive and display foam piece pre-installed. ket. Place the A08 Backlight Inverter on r edge is aligned to the top side and right

r Cable “P74” connector to location J1 on

’s ferrite bead into the molded saddle s not interfere with the saddle flange. (see

the hole from the back of the display and nt side.able, unlatch “CN101” connector lock on ive Display cable under latch with metal uit board until the cable is fully seated and e connector lock to secure the cable.

A1

illu



9-46




1 Active Display stallation (continued)

3. If replacing the A08 Backlight InverThe display bracket has the adhesRemove backing from display bracdisplay bracket so that J1 connectoedge of the bracket flange.

4. Connect the W17 Backlight InverteA08 Backlight Inverter.

5. Place W17 Backlight Inverter cablelocation such that the cable tie doeillustration 1).

6. Insert the snap rivet (266) throughensure the rivet expands on the fro

7. To install the W15 Active Display cA11 Active Display. Insert W15 Actcontact band facing toward the circsquare in the holding latches on th

W151

266

stration 3




F

A1In

te display backlight wires together around excess wires to the right, straight across

ide the display bracket.te the backlight wires from display along then back to the A08 Backlight Inverter.res to the A08 Backlight Inverter at J2.sembly in position in the front case. (If

ve the clear protective cover prior to

2033 must make contact with the thermal ase.

s (219) onto the top two screws (173); ding Harnesses Orientation for



9-47





8. A11 Active Display - 3309555, roublack strain relief features. Extendthe top of the display.

9. Position the A11 Active Display ins10. A11 Active Display - 3205278, rou

the corner and under the hook and11. Connect the A11 Active Display wi12. Place the active display bracket as

replacing the Active Display, remoinstalling it into the front case.)Note: A08 Backlight Inverter - 320conductive pad (201) on the front c

13. Place the two grounding harnessetorque to 6.8 in-lb. Refer to Groungrounding harness placement.




F

A1In

s (173) to secure the display assembly to

able to the A05 UI PCB at J36 (if removed

metal contacts down) into the connector

cure the cable.e square with the connector lock.

g the front case.



9-48





14. Install four new 4-40 0.312 screwthe front case; torque to 6.8 in-lb.

15. Connect the W15 Active Display Cpreviously), as follows. – Open the J36 connector lock.– Insert the W15 Display Cable (

lock.– Close the connector lock to seNote: The cable connector must b

16. Complete the process by Installin


arts List Interconnect Front Case View



F

A0PCMM

J2

2

9-49




8 Backlight Inverter B Diagram

IN 3202033IN 3308907 J1

J1J

3308907

Interconnect



F

A1DiM

CN2

9-50




1 Active Display agram IN 3205278

-000

W15 CN101

Interconnect



F

WCaM

28 AWG28 AWG28 AWG28 AWG28 AWG

P74

P74

9-51




17 Backlight Inverter ble Diagrams

IN 3200996

P37

P37

Interconnect



F

A0PC

t be removed before beginning this

from the A05 UI PCB at J31. from the A05 UI PCB at J32.0 0.312 screws (173) from the bottom the two grounding harnesses (221) r screws.ed grounding harnesses., transfer the grounding harnesses to the



9-52




5 User Interface (UI) B Removal

Note: The following assemblies musdisassembly:

– Top case– Front case– Active display assembly

To remove the A05 UI PCB:1. Disconnect the W18 UI Flex Cable2. Remove the Speed Dial connector3. Remove and discard the three 4-4

edge of the A05 UI PCB. Removeattached to the left and right corneNote: Replace any broken or frayNote: If replacing the A05 UI PCBnew PCB.




F

A0PC(c

12 screw (173) from the top left corner of

from the A05 UI PCB. Remove the two he center nut.front case.

A0PC front case.

from the W04 Speed Dial Assembly, and to the lower center stud, and install the UI PCB; torque nuts to 6.8 in-lb. Refer to for grounding harness placement.




9-53




5 User Interface (UI) B Removal

ontinued)

4. Remove and discard the 4-40 0.3the A05 UI PCB.

5. Remove the three 4-40 nuts (161) grounding harnesses attached to t

6. Remove the A05 UI PCB from the

5 User Interface (UI) B Installation

To install the A05 UI PCB:1. Position the A05 UI PCB onto the

2. Insert the grounding harness (246)a second grounding harness (219)three 4-40 nuts (161) onto the A05Grounding Harness Orientation





F

A0PC(c

s (221) onto the new lower left and right to 6.8 in-lb.s (173) onto the A05 UI PCB; torque to ess Orientation for grounding harness

ed grounding straps. the A05 UI PCB at J32. the A05 UI PCB at J31.g the active display assembly.


9-54




5 User Interface (UI) B Installation

ontinued)

3. Place the two grounding harnesse4-40 0.312 screws (173); torque

4. Install four new 4-40 0.312 screw6.8 in-lb. Refer to Grounding Harnplacement.Note: Replace any broken or fray

5. Install the Speed Dial connector to6. Connect the W18 UI Flex Cable to7. Complete the process by Installin




F

A0DiM(RM(n

35

6

7

J32 J34

J38 Pins 14 and 16

J33

9-55




5 User Interface PCB agramIN 3317230-002 oHS) orIN 3201966-007on-RoHS)

J

J3

J3J31

Interconnect



F

WDiM

A1

P21

Pin C1

Pin B1

Pin A1

Folded view

Pin A3

J22J21

9-56




18 UI Flex Cable agrams IN 3201000

P31

Fold lines

Pin 1

J31

Interconnect



F

WAs


bly:nnector from the A05 UI PCB at J32.

ve the Speed Dial knob (17).e Speed Dial axle.d Dial axle. Speed Dial Assembly out of the front

50) from the Speed Dial axle.


9-57




04 Speed Dial sembly Removal


To remove the W04 Speed Dial Assem1. Disconnect the W04 Speed Dial co2. Turn the front case over and remo3. Loosen and remove the nut from th4. Remove the washer from the Spee5. From inside the case, pull the W04

case.6. Remove the grounding harness (2




F

WAs

ly: onto the Speed Dial axle.04 Speed Dial Assembly into the front sembly to the notch in the front case.Dial axle.axle and torque to 10 in-lb.to the axle.mbly connector to the A05 UI PCB at J32.g the front case.


9-58




04 Speed Dial sembly Installation

To install the W04 Speed Dial Assemb1. Insert the grounding harness (250)2. From inside the case, install the W

case by aligning the key on the as3. Install the washer onto the Speed 4. Install the nut onto the Speed Dial 5. Press the Speed Dial knob (17) on6. Connect the W04 Speed Dial Asse7. Complete the process by Installin




F

WRe


: the W25 Speaker Harness Extension Speaker Harness Extension Cable s for more information. 0.312 screws (173) from the speaker the speaker mounting bracket from the

ly from the front case.


9-59




02 Speaker Assembly moval


– Top case– Front case

To remove the W02 Speaker Assembly1. Disconnect the speaker cable from

Cable connector. Refer to the W25removal and installation instruction

2. Remove and discard the two 4-40 mounting bracket (41), and removefront case.

3. Remove the W02 Speaker Assemb




F

WIn the front case and position the cable at

et (41) over the foam spacer and install ); torque to 6.8 in-lb.

25 Speaker Harness Extension Cable

g the front case.


9-60




02 Speaker Assembly stallation

To install the W02 Speaker Assembly:1. Fit the W02 Speaker Assembly into

the 2:00 position.2. Place the speaker mounting brack

two new 4-40 0.312 screws (1733. Connect the speaker cable to the W

connector. 4. Complete the process by InstallinW25

41




F

WAsM

J32

9-61




04 Speed Dial sembly Diagrams

IN 3201145

P32

Interconnect



F

WanHaCa

t case)

ker Harness Extension Cable (bottom case)86-000 (RoHS) or 3201593-003 (non-RoHS)

1

6

P05

J05

9-62




02 Speaker Assembly d W25 Speaker rness Extension ble Diagrams

W02 Speaker Assembly (fronMIN 3319086-001 (RoHS) or3201593-004 (non-RoHS)

W25 SpeaMIN 33190

Interconnect



B

As

BoBoA1ReA1InOEOEA0ReA0In

139

135

265

A01

2

29 (x5)

221(from Power Module)

278

W03 (from Bottom Case)

173(x2)

344

9-63



oardstack

sembly Diagram

Interconnect

ardstack Removalardstack Installation0 SpO2 Module moval0 SpO2 Module

stallationM/PP PCB RemovalM/PP PCB Installation1 System PCB moval1 System PCB

stallation

127

149 (x3)

A06

A10

161

A0

1

252 (x4)

252

173 (x5)

125

255

(x6)

258255262

255(x2)

W05 (from Bottom Case)



B

A0AsWMI32WMI32

A0■

A0In

A04

No longer

185 (x5)

161 (x3)

123 (x5)

145 (x3)

in assembly

9-64



oardstack (continued)

4 Therapy PCB sembly Diagramith Pacing:N 3317228-000 (RoHS) or 02259-010 (non-RoHS)ithout Pacing:N 3317228-001 (RoHS) or 02259-011 (non-RoHS)

4 Therapy PCB RemovalInductive Resistor

4 Therapy PCB stallation

139

147-

135 Ref

W07

229

A14

173

used

Interconnect



B

P


P Therapy View Main Assemblies

Ite NoteA0 B Part of kit MIN 3202718-044

3202718-047A0 B Part of kit MIN 3202718-029

(Non-RoHS)A0 B Part of kit MIN 3202718-038

(RoHS)A0 B Part of kit MIN 3202718-020

(non-RoHS)A0 cing) Part of kit MIN 3202718-035

(RoHS)A0 cing) Part of kit MIN 3202718-016

(non-RoHS)A0 t pacing) Part of kit MIN 3202718-036

(RoHS)

9-65




arts List

arts 123–173 Parts 185–344 System View

m Quantity MIN CAT. Part Description1 1 3317227-002 see note System Controller PC

1 1 3201964-015 see note System Controller PC

2 1 3317226-000 see note Patient Parameter PC

2 1 3202680-002 see note Patient Parameter PC

4 1 3317228-000 (P)

see note Therapy PCB (with pa

4 1 3202259-010 (P)

see note Therapy PCB (with pa

4 1 3317228-001 (w/o P)

see note Therapy PCB (withou



B

Pa


Pa Therapy View Main Assemblies

Ite NoteA0 pacing) Part of kit MIN 3202718-017

(non-RoHS)A0 pO2 Part of kit MIN 3202718-037

(RoHS)A0 pO2 Part of kit MIN 3202718-019

(non-RoHS)A1 Part of kit MIN 3202718-041

A1 Part of kit MIN 3202718-030

A1 NC Flash For devices with Masimo-Nellcor compatibility, Order kit MIN 3202718-031)

9-66

)





rts A01–W07 Parts 185–344 System View

m Quantity MIN CAT. Part Description4 1 3202259-011

(w/o P)see note Therapy PCB (without

6 1 3317224-000 (RoHS)

see note OEM Interface PCB (Smodels only)

6 1 3201950-004(non-RoHS)

see note OEM Interface PCB (Smodels only)

0 1 3318279 (RoHS)

see note SpO2 Module

0 1 3308709 (non-RoHS)

see note SpO2 Module

0 1 3318279 (RoHS)

see note SpO2 Module, with M



B

Pa


Ite NoteA1 NC For devices with Masimo-

Nellcor compatibility, Order kit MIN 3202718-031)

A1 ssemblyW Cable121212 Part of kit MIN 3202718-02112 hex, Part of kit MIN 3202718-021

13 r Part of kit MIN 3202718-040 (RoHS)

13 r Part of kit MIN 3202718-029 (non-RoHS)

9-67





m Quantity MIN CAT. Part Description0 1 3308709 (non-

RoHS)see note SpO2 Module, with M

Flash

4 1 3202773-000 21300-005068 Inductive Resistor A07 1 3202383-001 21300-004307 Capacitor Discharge3 5 3201374-010 21300-004242 ISO mount, Therapy5 1 202253-772 21300-006430 Screw 4-40 1.000L7 1 3200927-006 21300-004236 Boardstack shield9 5 3201375-006 21300-004815 Standoff-M/M 0.250

0.3755 1 3201007-002 21300-004704 Boardstack connecto

5 1 3201007-002 21300-004704 Boardstack connecto



B

Pa


It Note1 t

1 hex,

1 e pad No longer used in assembly

1 Part of kit MIN 3202718-0211 0

1 x 0.312L

1 x 0.500L

2

2 S, 4-40

2 0 x 0.312 3/32 hex drive

9-68





em Quantity MIN CAT. Part Description39 1 3200639 21300-004228 PCB support bracke

45 3 3201375-005 21300-004816 Standoff-M/M 0.250 0.250L

47 0 3201111-000 see note Thermally conductiv

49 3 3201374-011 21300-004243 ISO mount, OEM

61 9 200805-000 21300-000584 Locking hex nut, 4-4

73 3 202253-761 21300-001038 Machine screw, 4-40

85 5 202253-764 21300-004599 Machine screw, 4-40

29 2 200536-001 21300-000499 Cable tie retainer

52 5 201874-002 21300-008019 Machine screw, SEMx 5/16 L, Split

55 2 3202489-031 21300-005120 Screw-Cap, Hex,4-4Nylon

Pre Back Index Next Page


Bo

Par

Ite Note25 er Part of kit MIN 3202718-02126 Part of kit MIN 3202718-02126 12D

26 Part of kit MIN 3202718-040 (RoHS)

26 Part of kit MIN 3202718-029 (non-RoHS)

27 tack Part of kit MIN 3202718-021

34

Part Therapy View Main Assemblies

9-69

vious Page Table of Contents Section Contents


ardstack (continued)

ts List (continued)

m Quantity MIN CAT. Part Description8 1 3201374-012 21300-005187 ISO mount, Paramet

2 1 3203897-000 21300-006038 Nomex shield

4 2 200804-102 21300-000580 Washer, 0.125ID, 0.3

5 1 3201374-009 21300-005578 ISO mount, System Controller (standoff)

5 1 3201374-009 21300-005578 ISO mount, System Controller (standoff)

8 1 3206405-000 21300-006593 Shield - EMI, PCB S

4 1 202305-000 21300-001052 Coin cell battery, 3 V

s A01–W07 Parts 185–344 System View



B

BoDi

ly.only if it is being replaced).

B.

herapy View Main Assemblies

9-70




ardstack sassembly

To disassemble the boardstack:1. Remove the A07 Battery.2. Remove the top case.3. Remove the front case.4. Remove the boardstack assemb5. Remove the A10 SpO2 Module (6. Remove the A06 OEM/A02 PP PC7. Remove the A01 System PCB.8. Remove the A04 Therapy PCB.

Parts Lists Interconnect System View T



B

BoRe

plastic isolation mounts are cracking, then IN 3202718-021 as part of the

. emoved.



9-71




ardstack assembly

Note: If there are indications that the use the boardstack repair kit Mreassembly process.

To reassemble the boardstack:1. Install the A04 Therapy PCB.2. Install the A01 System PCB.3. Install the A06 OEM/A02 PP PCB4. Install the A10 SpO2 Module, if r5. Install the boardstack assembly.6. Install the front case.7. Install the top case.8. Install the A07 Battery.9. Review the labels parts list and in10. Complete the LIFEPAK 20 Device




B

Bo


erapy connectors are in view, and then set

(219) that connects the power module to removing the screw.ess if broken or frayed.nnector is in view.herapy Cable connector from the A04

assembly instructions to avoid a shock or


erapy View Main Assemblies

9-72




ardstack Removal .


To remove the boardstack assembly:1. Turn the device so the ECG and th

the device on its left side.2. Disconnect the grounding harness

the PCB support bracket (139) by Note: Replace the grounding harn

3. Turn the device so the ac power co4. Disconnect the 4-pin W10 Power/T

Therapy PCB at J17.

WARNINGSHOCK HAZARD. Carefully follow disdamage to wires during disassembly.

Parts Lists Interconnect System View Th



B

Bo(c

f its track and tilt it forward to make the

rom the A04 Therapy PCB at J16 by

ector Assembly from the A04 Therapy

charge Cable from the A04 Therapy PCB

cable at J13.nd therapy connectors are in view.e from the A01 System PCB at J8 by 3/32 allen driver.



9-73




ardstack Removal ontinued)

5. Lift the boardstack assembly out olower connections accessible.

6. Disconnect the W09 26-pin cable freleasing the outer tabs.

7. Disconnect the W01 Therapy ConnPCB at J14.

8. Disconnect the W07 Capacitor Disat J2.

9. Disconnect the therapy connector 10. Turn the device so that the ECG a11. Disconnect the W03 IrDA flex cabl

removing the screw (255) using a




B

Bo(c

ble from the A06 OEM/SpO2 Assembly at 5) using a 3/32 allen driver.ness from the A02 PP PCB at J23.ess Extension Cable from the

from the bottom case.stor’s cable from the A04 Therapy PCB

0.312 screws (173) that connect the A14 d (274) and PCB support bracket (139). from the bottom case.

OEM/SpO2 flex cable is secured to the locking post simultaneously to avoid


9-74




ardstack Removal ontinued)

12. Disconnect the W05 SpO2 Flex CaJ54 by first removing the screw (25

13. Disconnect the W06 ECG wire har14. Disconnect the W25 Speaker Harn

A01 System PCB at J5.15. Lift the boardstack assembly away16. Disconnect the A14 Inductive Resi

at J1.17. Remove and discard the two 4-40

Inductive Resistor to the EMI shiel18. Remove the boardstack assembly

CAUTIONPossible component damage. Thelocking posts. Remove the plug and damage to the connector.




B

Boconnector is visible, and lower the The boardstack assembly will not seat in ires do not slide into the notch cut for

the inductive resistor bracket (141).t (141) onto the PCB support bracket screws (173); torque to 6.8 in-lb. The h the top hole of the EMI shield (274).r’s cable to the A04 Therapy PCB at J1. erapy Cable as shown on the next page.Discharge Cable to the inductive resistor

r’s cable to the A04 Therapy PCB at J2.e Cable with the A14 Inductive Resistor’s ges.



9-75




ardstack Installation To install the boardstack assembly:1. Turn the device so that the power

boardstack assembly into its track.the tracks correctly if the therapy wthem in the boardstack assembly.

2. Place the A14 Inductive Resistor in3. Install the inductive resistor bracke

(139) using two new 4-40 0.312 bottom bracket screw goes throug

4. Connect the A14 Inductive ResistoRoute the cable under the W01 Th

5. Tie wrap (229) the W07 Capacitor bracket (141).

6. Connect the A13 Energy Capacito7. Route the W07 Capacitor Discharg

cable as shown on the following pa




BBo(c

or to the A04 Therapy PCB at J13. Route rapy connector cable into the lower left

or cable has a fourth ferrite bead, 0474-008 (non-RoHS)), route this bead necting to J13

(Continued on next page)herapy View Main Assemblies

9-76




ardstack Installation ontinued)

8. Connect the 5-pin therapy connectthree ferrite beads of the 5-pin thecorner of the A04 therapy PCB.Note: If the 5-pin therapy connect(MIN 3200474-009 (RoHS) or 320above the battery well, prior to con




B

Bo(c

ctor to the A04 Therapy PCB at J14.ble to the A04 Therapy PCB at J16.

the bottom case.y Connector Assembly slides into the slot



9-77





.

9. Connect the 10-pin therapy conne10. Connect the W09 26-Pin Power Ca11. Seat the boardstack assembly into

Note: Ensure that the W01 Therapin the A04 Therapy PCB.

Capacitor discharge cable passes under the W01 Therapy Cable and wraps around the J13 connector.Position the therapy cable ferrites so that they will not damage the J13 connector




B

Bo(c

rapy Cable connector to the A04 Therapy

nd therapy connectors are in view.s Extension Cable to the A01 System

PP PCB at J23.cluded) to the OEM PCB at J54, fasten

en driver, and torque to 6.5 in-lb.d IrDA connectors to the sockets, and e sockets using steady pressure to avoid

to the A01 System PCB at J08, fasten en driver, and torque to 6.5 in-lb.) from the power module to the EMI shield ing new 4-40 0.312 screws (173);

g the front case.



9-78





12. Connect the 4-pin W10 Power/ThePCB at J17.

13. Turn the device so that the ECG a14. Connect the W25 Speaker Harnes

PCB at J5.15. Connect the ECG cable to the A0216. Connect the W05 SpO2 Cable (if in

with a screw (255) using a 3/32 allNote: Carefully align the SpO2 angently press the connectors into thdamage to the connector pins.

17. Connect the W03 IrDA Flex Cablewith a screw (255) using a 3/32 all

18. Install the grounding harness (219(274) and support bracket (139) ustorque to 6.8 in-lb.

19. Complete the process by Installin




B

WDiRe

s part of the capacitor replacement kit. Removal procedure to remove the cable.Installation procedure to install the


9-79




07 Capacitor scharge Cable placement

The W07 Capacitor Discharge Cable iComplete the A13 Energy Capacitor Complete the A13 Energy Capacitor cable.




B

A1DiM

9-80




4 Inductive Resistor agram IN 3202773

J01

P01

Interconnect



B

WDiDiM into pin 5 of P02

9-81




07 Capacitor scharge Cable agram IN 3202383

Capacitor Discharge Connector (tie-wrapped to Inductive Resistor)

Interconnect



BA1Re


al removal)

y removing the two nuts (161) and

0.312 screws (252) from the A10 SpO2

m the boardstack assembly.

A1In placement kit for the LIFEPAK 20 device.

position over the A06 OEM PCB.s (252) into the A10 SpO2 Module; torque

ecuring it to the A06 OEM PCB with the torque to 6.8 in-lb.g the front case.


9-82




0 SpO2 Module moval

Note: Remove the following assemb– Top case– Front case– Boardstack assembly (option

To remove the SpO2 Module:1. Remove the Nomex shield (262) b

washers (264).2. Remove and discard the four 4-40

Module.3. Lift the A10 SpO2 Module away fro

0 SpO2 Module stallation

To Install the A10 SpO2 Module: Note: Order correct SpO2 module re1. Position the A10 SpO2 Module into2. Install four new 4-40 0.312 screw

to 6.8 in-lb.3. Install the Nomex shield (262) by s

two washers (264) and nuts (161);4. Complete the process by Installin




B

A1Di

M

J03 to J52

9-83




0 SpO2 Module agram

IN 3206274

J01 to J53

Interconnect



B

A0anAs


l removal)and optional A06 OEM/SpO2 assemblies:ble from the A06 OEM/SpO2 Assembly at

ness from the A02 PP PCB at J23.937 screw (125). Remove the three 4-40 rameter PCB.06 OEM/SpO2 option, remove the Nomex ashers (264) and nuts (161).odule if replacing the A06 OEM PCB.B (OEM/SpO2) assembly away from the the PCB clears the lip on the frame in the



9-84




2 Patient Parameter d A06 OEM/SpO2 sembly Removal

Note: Remove the following assemb– Top case– Front case– Boardstack assembly (optiona

To remove the A02 Patient Parameter 1. Disconnect the W05 SpO2 Flex Ca

J54 by removing the screw (255).2. Disconnect the W06 ECG wire har3. Remove and discard the 4-40 0.

nuts (161) from the A02 Patient Pa4. If the device is equipped with the A

shield (262) by removing the two wNote: Remove the A10 SpO2 m

5. Lift the A02 Patient Parameter PCboardstack assembly. Ensure that lower right corner.




B

A0anAs(c

mount (258) installed in the A02 Patient is in good condition.06 OEM/SpO2 option:ISO mounts (149) installed in the A06 re in good condition.meter PCB from the A06 OEM/SpO2

rameter PCB or A06 OEM PCB, remove ld PCBs, note the condition, and install ce the isolated mounts if broken or


9-85




2 Patient Parameter d A06 OEM/SpO2 sembly Removal

ontinued)

6. Inspect the orange parameter ISOParameter PCB. Verify the mount

7. If the device is equipped with the Aa. Inspect the three, white, OEM

OEM PCB. Verify the mounts ab. Separate the A02 Patient Para

assembly at J24.Note: If replacing the A02 Patient Pa

the isolated mounts from the othem on the new PCBs. Replacracked.

258




B

A0anAs

nd optional A06 OEM/SpO2 assembly:SO mount (258) is installed on the A02 uare end facing out.06 OEM/SpO2 option:M ISO mounts (149) are installed on the ends facing out.eter to the A06 OEM/SpO2 assembly at

OEM/SpO2) PCB onto the five standoffs sure the standoffs are tight and in good rs the lip in the lower right corner and the

06 OEM/SpO2 option:, if previously removed.



9-86




2 Patient Parameter d A06 OEM/SpO2 sembly Installation

To install the A02 Patient Parameter a1. Make sure the orange parameter I

Patient Parameter PCB with the sq2. If the device is equipped with the A

a. Make sure the three, white, OEA06 OEM PCB with the square

b. Connect the A02 Patient ParamJ24.

3. Install the A02 Patient Parameter ((129) on the boardstack shield (encondition). Make sure the PCB clea60-pin connector seats correctly.

4. If the device is equipped with the Aa. Install the A10 SpO2 module




B

A0anAs(c

onto the OEM PCB by securing it with two torque to 6.8 in-lb. Make sure the fold on er left corner of the OEM PCB.61) and new 4-40 0.312 screw (252) .8 in-lb.

the A06 OEM/SpO2 option, make sure ith two nuts (161) along the left side only;

ts (161) and new 4-40 1.00 screw (125) B; torque to 6.8 in-lb.cluded) to the OEM PCB at J54 and

nnector to the sockets, and gently press ing steady pressure to avoid damage to

PP PCB at J23.g the front case.


9-87




2 Patient Parameter d A06 OEM/SpO2 sembly Installation

ontinued)

b. Install the Nomex shield (262) washers (264) and nuts (161);the Nomex shield is in the upp

c. Install the one remaining nut (1onto the OEM PCB; torque to 6

5. If the device is NOT equipped withthe boardstack shield is secured wtorque to 6.8 in-lb.

6. Install the three remaining 4-40 nuonto the A02 Patient Parameter PC

7. Connect the W05 SpO2 Cable (if infasten with a screw (255).Note: Carefully align the SpO2 cothe connectors into the sockets usconnector pins.

8. Connect the ECG cable to the A029. Complete the process by Installin




B

A0PCM(R32(n

J21

J22

9-88




2 Patient Parameter B Diagram

IN 3317226-000 oHS) or 02680-002 on-RoHS)

J24

J23

Interconnect



B

A0PCM(R32(n

J54

P24

9-89




6 OEM Interface B Diagram

IN 3317224-000 oHS) or 01950-004 on-RoHS)

J52

J53

Interconnect



B

CoRe lies before beginning this disassembly:

al removal)OEM/SpO2 assembly, if applicable)

eld (127).er is installed on the A01 System tive contacts visible on top of the battery) the side of the battery)

9-90




in Cell Battery placement Note: Remove the following assemb

– Top case– Front case– Boardstack assembly (option– A02 Patient Parameter PCB (

To replace the coin battery:1. Remove the patient parameter shi2. Identify which type of coin cell hold

Controller PCB: A) Keystone (posior B) Renata (positive contacts to



.B

cordance with Replacement Procedure ment Procedure B for Renata holder.

B) Renata holder (positive contacts are to the side of the coin cell battery)

le

9-91




3. Replace the coin cell battery in acA for Keystone holder, or Replace

A) Keystone holder (positive contacts visibon top of the coin cell battery)



B

e: of the Keystone coin cell battery holder nd or deform the positive contacts during ry holder is damaged, replacement of the

required.itive side of battery holder while using a f the battery closest to the negative side contacts) until the battery releases from

9-92




Replacement Procedure A - KeystonCaution: The positive contactsare easily damaged. Do not beremoval or insertion. If the batteA01 System Controller PCB is

1. Push battery gently toward the posflat screwdriver to lift up the edge oof the holder (opposite the positivethe holder.



B

4) by inserting battery (positive up) nd then pressing it into the negative side attery is fullyseated in the holder.

d, check the voltage on the coin cell eter to confirm that the battery is installed h the holder.

r PCB and A06 OEM PCB.

9-93




2. Install the new coin cell battery (34underneath the positive contacts aof battery holder. Ensure that the b

3. After the battery has been replacebattery holder circuit with a multi-mcorrectly and is making contact wit

4. Replace the PCB shield (127).5. Install the A02 Patient Paramete



B

reviously removed).g the front case.


9-94




6. Install the A10 SpO2 Module (if p7. Complete the process by Installin




B

sitive side of battery holder while using a f the battery closest to the negative side

ses from the holder.

9-95




Replacement Procedure B - Renata:1. Push battery gently towards the po

flat screwdriver to lift up the edge oof the holder until the battery relea



B

4) by inserting the side of the battery ontacts and then pressing it into the Ensure that the battery is fully seated in battery touches the positive contacts

d, check the voltage on the coin cell eter to confirm that the battery is installed h the holder.

r PCB and A06 OEM PCB.

9-96




2. Install the new coin cell battery (34(positive up) against the positive cnegative side of the battery holder.the holder and that the side of the

3. After the battery has been replacebattery holder circuit with a multi-mcorrectly and is making contact wit

4. Replace the PCB shield (127).5. Install the A02 Patient Paramete



B

reviously removed).g the front case.


9-97




6. Install the A10 SpO2 Module (if p7. Complete the process by Installin




B

A0Re


and A06 OEM/SpO2 assembly, if

ded standoffs (129) from the A01 System

ff (265) from the A01 System PCB. the PCB support bracket (139).

135) (connects the A01 System PCB J03 , and safeguard it for reuse.ay remain connected to the A04 Therapy

may fall out completely when the ure to account for it immediately.


9-98




1 System PCB moval

Note: Remove the following assemb– Top case– Front case– Boardstack assembly– A02 Patient Parameter PCB (

applicable)To remove the A01 System PCB:1. Remove the PCB shield (127).2. Remove and discard the five threa

PCB.3. Remove the round, snap-in stando4. Remove the A01 System PCB from5. Locate the 8-pin stack connector (

with the A04 Therapy PCB at J15)Note: The 8-pin stack connector mPCB or the A01 System PCB, or itA01 System PCB is removed. Be s

139

129 149(x5)




B

A0In PCB, ensure that the plastic standoff

end up, on the A01 System PCB.35) into the A04 Therapy PCB at J15.PCB over the PCB support bracket (139), et standoffs. As the A01 System PCB rt bracket standoffs and the pins on the seat with their connectors evenly. (129), long end up, into the support

insulated standoff in the lower right

d.ing it down the five threaded standoffs on



9-99




1 System PCB stallation

To install the A01 System PCB:1. If you are replacing the A01 System

(149) is correctly positioned, large 2. Insert the 8-pin stack connector (13. Carefully position the A01 System

and slide it down the support brackslides down, ensure that the suppo8-pin and 60-pin stack connectors

4. Install five new threaded standoffsbracket.Note: Do not install a screw in thecorner at this time.

5. Replace the coin battery if neede6. Install the PCB shield (127) by slid

the A01 System PCB.

139

129 149(x5)




B

A0In

r PCB and A06 OEM PCB assembly.reviously removed)..g the front case.


9-100




1 System PCB stallation (continued)

7. Install the A02 Patient Paramete8. Install the A10 SpO2 Module (if p9. Install the Boardstack Assembly10. Complete the process by Installin




B

A0DiM(R32(n

4

J03

J02

J01

9-101




1 System PCB agram IN 3317227-002 oHS) or 01964-015 on-RoHS)

Coin battery

J02

J08 J05 J0

J07

Interconnect



B

A0Re


0.312 screws (173) connecting the o the PCB support bracket (139). mbly (A14). 0.500 screws (185) located inside the

n with the A04 Therapy PCB.from the metal standoffs along the top illustration B at left).

m the PCB support bracket (139).135) (connecting the A01 System PCB at 5) and safeguard it for reuse.



9-102




4 Therapy PCB moval

Note: Remove the following assemb– Top case– Front case– Boardstack assembly

To remove the A04 Therapy PCB:1. Remove and discard the two 4-40

inductive resistor assembly (A14) t2. Remove the inductive resistor asse3. Remove and discard the five 4-40

five insulated standoffs. Note: The standoffs should remai

4. Remove the three 4-40 nuts (161) edge of the A04 Therapy PCB (see

5. Remove the A04 Therapy PCB fro6. Locate the 8-pin stack connector (

J3 with the A04 Therapy PCB at J1

A

B

173

A14

139

161

185

A04

(x5)

(x3)

278




B

A0Re

ay remain connected to the A04 Therapy may fall out completely when the ure to account for it immediately. PCB, remove the five insulated standoffs

ote the condition, and reinstall them, large CB.

A0In rt bracket (139), install three new

nto the bracket.CB, ensure that the five plastic standoffs e end up, on the PCB.stalled on the boardstack assembly, tor (135) and the 60-pin stack connector System PCB.



9-103




4 Therapy PCB moval (continued)

Note: The 8-pin stack connector mPCB or the A01 System PCB, or itA01 System PCB is removed. Be sNote: If replacing the A04 Therapy(149) from the old Therapy PCB, nend up, on the new A04 Therapy P

4 Therapy PCB stallation

To install the A04 Therapy PCB:1. If you are replacing the PCB suppo

standoffs (145), short side down, o2. If you are replacing the Therapy P

(149) are correctly positioned, largNote: If the A01 System PCB is inensure that the 8-pin stack connecare securely positioned on the A01




B

A0In

B with the PCB support bracket (139) 04 Therapy PCB slides down the support pins on the 8-pin and 60-pin stack ors evenly.s (185) in the five insulated standoffs

to the metal standoffs along the top edge 6.8 in-lb.bly (A14) onto the PCB support bracket screws (173); torque to 6.8 in-lb. The gh the top hole of the EMI shield (278). cable under the W01 Therapy Cable, the ischarge Cable (see illustration)..g the front case.


9-104




4 Therapy PCB stallation (continued)

3. Carefully align the A04 Therapy PCand press it into position. As the Abracket standoffs, ensure that the connectors seat with their connect

4. Install five new 4-40 0.500 screw(149); torque to 6.8 in-lb.

5. Install the three 4-40 nuts (161) onof the A04 Therapy PCB; torque to

6. Install the inductive resistor assem(139) using two new 4-40 0.312 bottom bracket screw will go throu

7. Route the A14 Inductive Resistor’ssame way as the W07 Capacitor D

8. Install the Boardstack Assembly9. Complete the process by Installin




B

A0DiM(R32(n


J01

J02

J17

Therapy Pacer Simm PCB

9-105




4 Therapy PCB agram (With Pacing)IN 3317228-000 oHS) or 02259-010 on-RoHS)

J15

J13

J14J16

Interconnect



B

As(M

Part Connectors View Main Assemblies

BoBoA1A1■

■

■

■

A0A0A1ReA1In

105 (x4)

f

A13(x2)

162

23895 (x2)

173 (x10)

(A)12225

W09

99A03

89

tail B

221

A07103

227

159

22 (part of kit320718-024)(x2)

9-106



ottom Case

sembly Diagram odules)

s A03–W09 Parts W10–95 Parts 99–183 Parts 221–270

ttom Case Disassemblyttom Case Reassembly2 Printer Module Removal2 Printer Module InstallationPrinterPrinter flex cablePrinter bezelPrinter shroud

3 Power Module Removal3 Power Module Installation3 Energy Capacitor moval3 Energy Capacitor

stallationBottom View

Detail B

241 Center Between Terminals

241 Re

93

W14

A12

See De

83

12 (E)

A07 Connection

12(F) SpO2

183 270LIFEPAK 20e

device Only

LIFEPAK 20e Only

W13

W08

W10



B

As(C

Pa Module View Main Assemblies

159

W01

W25

A0WWInWWWWWW

Ref

268

9-107



ottom Case (continued)

sembly Diagram onnectors)

rts A03–W09 Parts W10–95 Parts 99–183 Parts 221–270

W06

113

W03

111

173 (x2)

W05 (x2)229

7 Battery Replacement01 Therapy Connector Removal01 Therapy Connector stallation06 ECG Connector Removal06 ECG Connector Installation05 SpO2 Connector Removal05 SpO2 Connector Installation03 IrDA Assembly Removal03 IrDA Assembly Installation

SpO2 Only



B

Pa


P Connectors View Main Assemblies

Ite Note

A K 20 Part of kit MIN 3202718-010

A K 20e Part of kit MIN 3202718-039 (RoHS)

A K 20e Part of kit MIN 3202718-022 (non-RoHS)

A , LIFEPAK 20

A AK 20e

A nthead

A nthead

A Part of kit MIN 3202718-025

W ly Part of kit MIN 3202718-043 (RoHS)

9-108




rts List

arts W10–95 Parts 99–183 Parts 221–270 Module View


03 1 3202131-010 see note Power Module Assy, LIFEPA

03 1 3317740-000 (RoHS)

see note Power Module Assy, LIFEPA

03 1 3202131-009 (non-RoHS)

see note Power Module Assy, LIFEPA

07 1 3200497-001 11141-000068 12V, 3Ah, NiMH battery pack

07 1 3205296 11141-000112 Battery Pack – Li-ion, LIFEP

12 1 3318747-000 (RoHS)

21240-000003 Printer - 50MM, Thermal Pri

12 1 3200920-000(non-RoHS)

21240-000001 Printer - 50MM, Thermal Pri

13 1 3200846 see note Energy Storage Capacitor

01 1 3200474-009 (RoHS)

see note Therapy Connector Assemb



B

PaIte Note

W ly Part of kit MIN 3202718-026 (non-RoHS)

W

W

W Part of kit MIN 3202718-013

W

W

W Part of kit MIN 3202718-039 (RoHS)

W Part of kit MIN 3202718-022 (non-RoHS)

9-109





rts List (continued)m Quantity MIN CAT. Part Description

01 1 3200474-008 (non-RoHS)

see note Therapy Connector Assemb

03 1 3200926-007 (RoHS)

21300-008131 IrDA Flex Assembly

03 1 3200926-006(non-RoHS)


05 1 3200925-006 21300-004234 SpO2 Flex Assembly

06 1 3318315 (RoHS)

21330-001521 ECG 7-Contact Receptacle

06 1 3201010-009 (non-RoHS)

21300-004239 ECG 7-Contact Receptacle

08 1 3206579-001 21330-001166 Battery Cable, LIFEPAK 20e

08 1 3206579-001 21330-001166 Battery Cable, LIFEPAK 20e



B

Pa


Par Connectors View Main Assemblies

Ite Note

W ble

W PAK 20e Part of kit MIN 3202718-039 (RoHS)

W PAK 20e Part of kit MIN 3202718-022 (non-RoHS)

W Part of kit MIN 3202718-039 (RoHS)

W Part of kit MIN 3202718-022 (non-RoHS)

W 20e Part of kit MIN 3202718-039 (RoHS)

W 20e Part of kit MIN 3202718-022 (non-RoHS)

W y

9-110





ts A03–W09 Parts 99–183 Parts 221–270 Module View


09 1 3201241-000 21300-004669 Power to Therapy 26-pin Ca

10 1 3206857-000 21330-001165 Power/Therapy Cable, LIFE

10 1 3206857-000 21330-001165 Power/Therapy Cable, LIFE

11 1 3201997 see note ECG Sync/System Cables

11 1 3201997 see note ECG Sync/System Cables

13 1 3206469-003 21330-001164 AC Power Cable, LIFEPAK

13 1 3206469-003 21330-001164 AC Power Cable, LIFEPAK

14 1 3201001-006 21300-008058 Printer Flex Cable Assembl



B

Pa



Ite Note

W Ext.

W Ext.

12 K 20 Refer to Labels Assembly

12 K 20e Refer to Labels Assembly

22 8 Part of kit MIN 3202718-024

83

89

93 ssy)


9-111





ts A03–W09 Parts W10–95 Parts 221–270 Module View


25 1 3319086-000 (RoHS)

21300-008132 Speaker Assembly Harness

25 1 3201593-003(non-RoHS)

21300-004246 Speaker Assembly Harness

sheet 3201640 see note Label Set (6 labels), LIFEPA

sheet 3206034 see note Label Set (6 labels), LIFEPA

2 3202228-562 21300-003883 Standoff-Hex, M/F,4-40,0.18

1 3201408-000 21300-004621 Printer Bezel

1 3200626-004 21300-004306 Printer Shroud

2 804447-36 21300-007458 Foam Spacer (part of A13 a

2 3200922-000 21300-004619 Capacitor Support Bracket



B

Pa


Ite Note

99

10

10 e

10 Part of bottom case assembly

11 Part of kit MIN 3202718-043 (RoHS)

11 Part of kit MIN 3202718-026 (non-RoHS)

11 Clip Part of kit MIN 3202718-013

15

16 13 assembly) Part of kit MIN 3202718-025

17 12L

9-112








1 3201597-000 21300-004653 EMI Foam Core Gasket

3 1 3200628-002 21300-004835 Battery Door, LIFEPAK 20

3 1 3200628-004 21300-006412 Battery Door, LIFEPAK 20

5 4 802885-00 21300-002137 Mounting Foot

1 1 200040-001 21300-000149 Therapy Retaining Ring

1 1 200040-001 21300-000149 Therapy Retaining Ring

3 1 3200921-000 21300-004602 SpO2 Connector Mounting

9 1 3200625-006 21300-004889 Bottom case assembly

2 1 3009787-003 21300-004110 Capacitor shield (part of A

3 12 202253-761 21300-001038 Machine screw 4-40 0.3



B

Pa


Ite Note

18 PAK 20 Refer to Labels Assembly

18 PAK 20e Refer to Labels Assembly

22

22

22 Attached to battery door (103)




26 Mount Part of kit MIN 3202718-043 (RoHS)

26 Mount Part of kit MIN 3202718-026 (non-RoHS)

27 ning LIFEPAK 20e only

9-113







3 1 3201643-012 see note Serial number label, LIFE

3 1 3201643-016 see note Serial number label, LIFE

1 1 3202246-004 21300-004255 Grounding strap harness

5 1 3202377-010 21300-004400 Plastic Fastener

7 1 802885-01 21300-002138 Mounting foot

9 2 200536-001 21300-000499 Cable tie retainer

8 1 3206900-001 21300-006962 Dielectric shield

1 1 3300694-000 21300-007794 Poron Foam, Capacitor

8 1 3203445-001 21300-005784 Seal, Therapy Connector

8 1 3203445-001 21300-005784 Seal, Therapy Connector

0 1 3206152-000 21501-001625 Label, NIMH Battery War



B

BoDi

ly..or.

ctor.r.or.r.ss Extension Cable.


9-114




ttom Case sassembly

To disassemble the bottom case:1. Remove the A07 Battery.2. Remove the top case.3. Remove the front case.4. Remove the boardstack assemb5. Remove the A12 Printer Module6. Remove the A13 Energy Capacit7. Remove the A03 Power Module.8. Remove the W01 Therapy Conne9. Remove the W06 ECG Connecto10. Remove the W05 SpO2 Connect11. Remove the W03 IrDA Connecto12. Remove the W25 Speaker Harne

arts List Interconnect Diagram Module View



B

BoRe cing case).

friction foot pads (105), as needed.ot (227) to the battery door (103), as

Extension Cable.

.

tor.

.



9-115




ttom Case assembly

To reassemble the bottom case:1. Obtain a new bottom case (if repla2. Inspect and install the bottom case3. Inspect and install the mounting fo

needed.4. Install the W25 Speaker Harness5. Install the W03 IrDA Connector.6. Install the W05 SpO2 Connector7. Install the W06 ECG Connector.8. Install the W01 Therapy Connec9. Install the A03 Power Module.10. Install the A13 Energy Capacitor11. Install the A12 Printer Module.12. Install the boardstack assembly.




B

BoRe(c



9-116




ttom Case assembly

ontinued)

13. Install the front case.14. Install the top case.15. Install the A07 Battery.16. Review the labels parts list and in17. Complete the LIFEPAK 20 Device




B

A1Re

embly and shroud:r Flex cable is remove, the following mbly:

the printer paper roll.cated inside the printer on the rear wall.f the printer shroud (89).able from the printer at printer

sembly instructions to avoid a shock or embly.



9-117




2 Printer Module moval

To remove the A12 Printer Module assNote: If Printer shroud or W14 Printe

assemblies will require disasse– A07 Battery– Top case– Front case– Boardstack

1. Open the printer door and remove2. Loosen the two captured screws lo3. Carefully pull the A12 Printer out o4. Disconnect the W14 Printer Flex C

connection J1.

W14

173

89

(x3)

WARNINGSHOCK HAZARD. Carefully follow disascausing damage to wires during disass




B

A1Re

the removal process is complete. If W14 Printer Flex Cable, continue with the art is removed.

away from the bottom case.0 0.312 screws (173) from the bottom of

he 4-pin power cable. from the A03 Power Module at J45, and tout.e W14 Printer Flex Cable through the

m the bottom case.way and carefully remove the W14 Printer he cable is held in place by adhesive, so id damaging the connectors or the cable.


9-118




2 Printer Module moval (continued)

Note: If removing the A12 Printer,removing the printer shroud or the removal process until the desired p

5. Slide the printer bezel (83) up and6. Remove and discard the three 4-4

the printer shroud (89).7. Carefully lift the shroud to access t8. Disconnect the 4-pin power cable

feed it through the small shroud cu9. Feed the 4-pin power cable and th

large shroud cutout.10. Remove the printer shroud (89) fro11. Lift the W06 ECG Cable out of the

Flex Cable from the bottom case. Tit should be removed evenly to avo




B

A1In

, start at step 9.

nder the W06 ECG Cable and position the f the guide on the bottom case.nd the 4-pin power cable connector .rough the small slot in the shroud.r to the A03 Power Module at J45, tioned correctly.the bottom case.ws (173) into the bottom of the printer



9-119




2 Printer Module stallation

Note: If installing the A12 Printer onlyTo install the printer module:1. Slide the W14 Printer Flex Cable u

printer cable along the right side o2. Insert the printer cable connector a

through the large slot in the shroud3. Insert the 4-pin power connector th4. Connect the 4-pin power connecto

ensuring that the connector is posi5. Position the printer shroud (89) in 6. Install three new 4-40 0.312 scre

shroud; torque to 6.8 in-lb.

W14

173

89

(x3)




B

A1In

) into the printer shroud to secure the J45

g that it is flush with the bottom case.le to the J1 connector on the printer. The ar of the printer.able lays between the two captured

r shroud. cated in the A12 Printer and torque to

ter and close the printer door.

PIP.


9-120




2 Printer Module stallation (continued)

7. If removed, press the fastener (225flex connector.

8. Insert the printer bezel (83) ensurin9. Connect the W14 Printer Flex Cab

cable should lay flat against the re10. Ensure that the W14 Printer Flex C

screws.11. Slide the A12 Printer into the printe12. Tighten the two captured screws lo

10 in-lb.13. Install the paper roll in the A12 Prin14. Install the boardstack.15. Install the front case.16. Install the top case.17. Install the A07 Battery.18. Complete the LIFEPAK 20 Device

83

A12




B

WDiM

Pin 2Pin 1

Pin 40Pin 39

etail B

Detail A

see Detail A

9-121




14 Printer Flex Cable agrams IN 3201001

Pin 2Pin 4

Pin 3

Detail C

Pin 1

fold-up lines

Adhesive tape (center on flex)

fold-up lines

see Dsee Detail C

Detail B

Interconnect



BA1Re


t removed, remove and discard the screw

y Cable from the A04 Therapy PCB at

y from the printer shroud (89) and the

r Discharge Cable from the A04 Therapy




9-122




3 Energy Capacitor moval

Note: Remove the following assemb– A07 Battery– Top case– Front case

To remove the A13 Energy Capacitor:1. If the boardstack assembly was no

and ground cable (221).2. Disconnect the W10 Power/Therap

J17.3. Pull the boardstack assembly awa

power module.4. Disconnect the W07/A13 Capacito

PCB at J2.





B

A1Re

e adjacent hardware or wires when arge Cable.) securing the W07 Capacitor Discharge ket (141). 0.312 screws (173) from the rear of the

apacitor brackets.foam tape (162 and 93) from the

(95), remove and discard the two 4-40 f the capacitor brackets (95) and remove capacitor shield (238) (see illustration on


9-123




3 Energy Capacitor moval (continued)

Note: Take care not to damage thremoving the W07 Capacitor Disch

5. Remove the cable tie retainer (229Cable to the inductive resistor brac

6. Remove and discard the two 4-40 capacitor brackets (95).

7. Lift the capacitor (A13) out of the c8. Remove the capacitor sleeve with

capacitor.9. If removing the capacitor brackets

0.312 screws (173) from the front othe capacitor brackets (95) and thenext page).

A13

95 173(x2)




B

A1In standoffs (22) are on the power module.

d the two capacitor brackets (95) onto the 12 screws (173); torque to 6.8 in-lb (if the

ensuring that the plastic sleeve and poron ecurely.wrapped tightly around the capacitor, with acitor. Poron tape must secure the sleeve

to ensure that foam tape (240) is present

itor brackets (95) with the capacitor cable the warning label visible at the top of the

s (173) into the capacitor brackets; torque



9-124




3 Energy Capacitor stallation

To install the A13 Energy Capacitor:1. Ensure that two capacitor bracket 2. Install the capacitor shield (238) an

standoffs using two new 4-40 0.3brackets were removed).

3. Inspect the A13 Energy Capacitor tape are positioned correctly and sNote: The plastic sleeve must be the wrap joint at the top of the capat both ends of the capacitor.

4. Inspect the A13 Energy Capacitor (optional on LIFEPAK 20 device).

5. Install the capacitor into the capacend toward the printer shroud and capacitor.

6. Install two new 4-40 0.312 screwto 6.8 in-lb.

238

95173

22

240 Center Between Terminals




B

A1In

ts are centered on the poron tape connect rapy PCB at J2. The W07 Capacitor 4 of this connector.ge Cable to the inductive resistor bracket ). Route the cable over the A04 Therapy llustration) as the inductive resistor

stalled.lled. herapy Cable connector to the A04 oardstack assembly.73) and fasten the ground cable (221) to

PIP.


9-125




3 Energy Capacitor stallation (continued)

7. Ensuring that the capacitor brackethe capacitor cable to the A04 TheDischarge Cable is attached at pin

8. Secure the W07 Capacitor Dischar(141) with a cable tie retainer (229PCB using the same routing (see icables.

9. Install the power module, if not in10. Install the boardstack, if not insta11. Reconnect the 4-pin W10 Power/T

Therapy PCB at J17. Reseat the b12. Install a new 4-40 0.312 screw (1

the boardstack; torque to 6.8 in-lb.13. Install the front case.14. Install the top case.15. Install the A07 Battery.16. Complete the LIFEPAK 20 Device




B

A0Re


l)y:lled in the bottom case, continue with has been removed, proceed to step 5.y Cable from the A04 Therapy PCB at

from the A04 Therapy PCB at J16.




9-126




3 Power Module moval

Note: Remove the following assemb– A07 Battery– Top case– Printer module– Capacitor (optional removal)– Boardstack (optional remova

To remove the power module assembl1. If the boardstack assembly is insta

step 2. If the boardstack assembly2. Disconnect the W10 Power/Therap

J17.3. Disconnect the W09 26-Pin Cable





B

A0Re

y from the printer shroud and power

ove the A13 Energy Capacitor

ght 4-40 0.312 screw (173) that secures and grounding harness (221).ess (221) as you remove the right forward ess if broken or frayed.ft 4-400.312 screw (173) that secures

(173) that secures the right rear corner

le up, clearing the loosened screw, and


9-127




3 Power Module moval (continued)

4. Pull the boardstack assembly awamodule.

5. If replacing the power module, rem(complete steps 6 through 9).

6. Remove and discard the forward rithe right side of the power moduleNote: Remove the grounding harnscrew. Replace the grounding harn

7. Remove and discard the forward lethe left side of the power module.

8. Loosen the rear 4-400.312 screwof the power bracket three turns.

9. Tilt the left side of the power moduremove it from the bottom case.




BA0In 400.312 screw (173) is loosely installed

case.ottom case ensuring that the notch in the the loosened screw.73) in the power bracket’s left forward

rough the grounding strap (221) ring, and ket’s right forward corner; torque to 6.8 in-

the grounding strap.3) in the rear right corner; torque to 6.8 in-

, if it was removed.moved.tween the A03 Power Module at J41 and



9-128




3 Power Module stallation

To install the power module assembly:1. Ensure that the right rear corner 4-

(back off 3 to 5 turns) in the bottom2. Position the power module in the b

rear right lip slips into place under 3. Install a new 4-400.312 screw (1

corner; torque to 6.8 in-lb.4. Insert a 4-400.312 screw (173) th

install the screw in the power braclb.Note: If broken or frayed, replace

5. Tighten the 4-400.312 screw (17lb.

6. Install the A13 Energy Capacitor7. Install the boardstack, if it was re8. Connect the W09 26-Pin Cable be

the A04 Therapy PCB at J16.




B

A0In

rapy Cable connector to the A04 Therapy

PIP.


9-129




3 Power Module stallation (continued)

9. Connect the 4-pin W10 Power/ThePCB at J17.

10. Install the A12 Printer Module.11. Install the front case.12. Install the top case.13. Install the A07 Battery.14. Complete the LIFEPAK 20 Device




B

A0DiM(R32(n

J41J48

9-130




3 Power Module agramIN 3317740-000 oHS) or 02131-010 on-RoHS)

1

J45 J4712

J49

J51J50

12

1

1

Interconnect



B

WDi(LM

J50

A03

9-131




08 Battery Cable agramsIFEPAK 20e Only) IN 3206579

J85

A07

Interconnect



B

WDiM Pin 1

J16

P161

26

9-132




09 26-Pin Cable agramsIN 3201241 Pin 1

J41

P411

26

Interconnect



B

WCa(LM

J51

9-133




10 Power/Therapy ble Diagrams

IFEPAK 20e Only)IN 3206857

J17

Interconnect



B

WCaM J47

P47

- ECG Analog Out - Ground

External Sync In Ground

9 - +5 volts DC out

6 - RS232 -DTR

8 - RS232 -RTS

2 - RS232 -TX

7 - RS232 -CTS

5 - Ground

3 - RS232 -RX

9-134




11 ECG Sync/System bles Diagrams

IN 3201997 DB-9

DB-15

1514

6 -5 -

Interconnect



B

WDi(LM

J49

9-135




13 AC Power Cable agrams IFEPAK 20e Only)IN 3206469

J43

Interconnect



B

WRe


0.312 screws (173) from the W06 ECG ase assembly. W06 ECG Connector from the bottom

ugh the connector hole.


9-136




06 ECG Connector moval


– A07 Battery– Top case– Front case– Boardstack

To remove the W06 ECG Connector:1. Remove and discard the two 4-40

Connector located on the bottom c2. From outside the case, remove the

case and feed the ECG cable thro




B

WIn e W06 ECG Connector with the connector

onnector with the notch in the bottom into position. s (173) into the W06 ECG Connector;

en the first rib and the forward left corner

t in the bottom case.

PIP.


9-137




06 ECG Connector stallation

To install the W06 ECG Connector:1. On the outside of the case, align th

standoffs and align the key in the ccase and slide the ECG connector

2. Install two new 4-400.312 screwtorque to 6.8 in-lb.

3. Position the cable in the slot betweof the bottom case.

4. Place the first ferrite bead in its slo5. Install the boardstack.6. Install the front case.7. Install the top case.8. Install the A07 Battery.9. Complete the LIFEPAK 20 Device




B

WAsM(R32(n ECG Connector,

Inside View

9-138




06 ECG Connector sembly Diagrams

IN 3318315oHS) or 01010-009 on-RoHS)

J23

Interconnect



B

WCo


r Assembly:eal (268) from the W01 Therapy

m the back of the W01 Therapy

therapy connector from the bottom case the connector hole.


9-139




01 Therapy nnector Removal



To remove the W01 Therapy Connecto1. Remove the Therapy Connector S

Connector.2. Remove the retaining ring (111) fro

Connector.3. From outside the case, remove the

and feed the therapy cable through




B

WCo

Assembly:y on the connector with the notch in the

erapy Connector Assembly into the

the back of the W01 Therapy Connector at the open end is visible.l (268) onto the W01 Therapy Connector.

PIP.


9-140




01 Therapy nnector Installation

To install the W01 Therapy Connector 1. From outside the case, align the ke

bottom case and slide the W01 Thbottom case.

2. Install the retaining ring (111) onto Assembly, and rotate the clip so th

3. Install the Therapy Connector Sea4. Install the boardstack.5. Install the front case.6. Install the top case.7. Install the A07 Battery.8. Complete the LIFEPAK 20 Device




B

WCoDiM(R32(n

4 5 6

10 11

3 7

9 12

812

9-141





agrams IN 3200474-009 oHS) or 00474-008 on-RoHS)

J13

J14

P14

P13

Interconnect



B

WCoW

ApexSternum+5v (vcc)Discharge switchCharge switchCharge LEDRecord switchEnergy selectCable sense (0)Cable sense (1)Cable parityCommon (Gnd)

731284569101112

9-142





iring DiagramWHT

WHT

NCNCNC

BRNREDORNYELGRNBLUVOIGRYWHTBLK

52347

12345678910

ferrite beads

ferrite beads

Interconnect



B

WRe


ssembly:) securing the SpO2 cable to the bottom removed to expose this tie wrap.rms on the SpO2 connector mounting clip

e bottom case.mbly away from the bottom case.


9-143




05 SpO2 Connector moval


– A07 Battery– Top case– Front case– Boardstack– W03 IrDA Port

To remove the W05 SpO2 Connector A1. Remove the cable tie retainer (229

case. The W03 IrDA Port must be 2. Gently pull apart the plastic snap a

(113), away from the bottom case.3. Lift the mounting clip away from th4. Lift the W05 SpO2 connector asse




B

WIn

sembly:tor into the locating detail in the bottom

ting clip (113) in front of the mounting

g clip in and down onto the bottom case p arms click into position.ecure the ferrite bead to the bottom case.

PIP.



9-144




05 SpO2 Connector stallation

To install the W05 SpO2 Connector As1. Place the W05 SpO2 input connec

case.2. Position the SpO2 connector moun

block detail on the bottom case.3. Press the SpO2 connector mountin

mounting block detail until the sna4. Install a cable tie retainer (229) to s5. Install the W03 IrDA Assembly.6. Install the boardstack.7. Install the front case.8. Install the top case.9. Install the A07 Battery.10. Complete the LIFEPAK 20 Device




B

WDiM

fold up here

fold up here fold up here

Folding dimensions

Back view

9-145




05 SpO2 Assembly agramsIN 3200925

Interconnect

P54P83

123456789

10

1413121110987654321

DET_ANODEDET_CATHODE

IR_CATHODE

RED_CATHODE

OUTER SHIELD

INNER SHIELD

Schematic diagram

1615 (MNTG-HOLE)

(MNTG-HOLE)

Front view Side view



B

WRe


l)

isconnect the W03 IrDA flex cable from removing the screw (255) using a 3/32

slot between the bottom case cutout (A)

driver. Bend the right IrDA snap tab (B) dge of the W03 IrDA Assembly.rom the bottom case. the bottom case, disconnect the IrDA

B at J8.


9-146




03 IrDA Assembly moval


– A07 Battery– Top case– Front case– Boardstack (optional remova

To remove the W03 IrDA Assembly:1. If the boardstack is not removed, d

the A01 System PCB at J8 by firstallen driver.

2. Insert a slotted screwdriver into theand the right snap tab (B).

3. Gently apply pressure to the screwoutward slightly, freeing the right e

4. Remove the W03 IrDA Assembly f5. If the boardstack is still installed in

connector from the A01 System PCB

A




B

WIn n the bottom case. (The IrDA is located

n the bottom case.)to the slot between the bottom case ).driver. Bend the right IrDA snap tab (B)

n into the snap tabs and release the nap tabs will close around the W03 IrDA

ly is resting centered on the support

o the A01 System PCB at J08 and fasten en driver, if the boardstack is still installed tall the boardstack. The IrDA flex cable installation.



9-147




03 IrDA Assembly stallation

To install the W03 IrDA Assembly:1. Position the W03 IrDA Assembly o

near the center of the front panel o2. Insert a large slotted screwdriver in

cutout (A) and the right snap tab (B3. Gently apply pressure to the screw

slightly outward, 4. Press the W03 IrDA Assembly dow

pressure on the screwdriver. The sAssembly.

5. Ensure that the W03 IrDA Assembbrackets and snap tabs.

6. Connect the W03 IrDA Assembly twith a screw (255) using a 3/32 allin the bottom case. Otherwise, Insis connected during the boardstack

B

A




B

WIn

PIP.


9-148




03 IrDA Assembly stallation (continued)

7. Install the front case.8. Install the top case.9. Install the A07 Battery.10. Complete the LIFEPAK 20 Device




B

WDiM(R32(n

three-dimensional view

9-149




03 IrDA Assembly agramsIN 3200926-007 oHS) or 00926-006 on-RoHS)

side viewfront view

Interconnect



B

WExRe


arness Extension Cable:ess Extension Cable from the W02 se removal).25 Speaker Harness Extension Cable art of boardstack removal).uring the ferrite ring to the bottom case.lder and feed the W25 Speaker Harness erapy Connector Assembly. Remove the C


9-150




25 Speaker Harness tension Cable moval



Note: To remove the W25 Speaker H1. Disconnect the W25 Speaker Harn

Speaker Assembly (part of front ca2. Disconnect the other end of the W

from the A01 System PCB at J5 (p3. Cut the cable tie retainer (229) sec4. Remove the connector from the ho

Extension Cable under the W01 Thcable from the bottom case.

able tie retainer




B

WExIn

xtension Cable:xtension Cable under the W01 Therapy

xtension Cable into the holder in the

n the set of holes 0.5 inches to the left of mbly, and secure the extension cable’s

PIP.


9-151




25 Speaker Harness tension Cable

stallation

To Install the W25 Speaker Harness E1. Feed the W25 Speaker Harness E

Connector Assembly.2. Insert the W25 Speaker Harness E

bottom case.3. Install the cable tie retainer (229) i

the W01 Therapy Connector Asseferrite ring to the bottom case.

4. Install the boardstack.5. Install the front case.6. Install the top case.7. Install the A07 Battery.8. Complete the LIFEPAK 20 Device




F

DeIn3232

he device with isopropyl alcohol.age).age for placement):

NoteA in Labels Assembly diagram

NG B in Labels Assembly diagram

NG B in Labels Assembly diagram

el C in Labels Assembly diagramD in Labels Assembly diagramE in Labels Assembly diagramF in Labels Assembly diagramSelect languageSN label illustration

ENG Select language

9-152



inal Assembly

vice Labeling cluding Label Set (12) 01640 - LIFEPAK 20 06034 - LIFEPAK 20e

To apply the labels to the device:1. Remove the old labels and clean t2. Select the correct label set (langu3. Apply the labels (refer to the next p

Item MIN (ref) Part Description12 - Label set 3201290 Rear connector label12 - Label set 3201274-030 Front connector label, E

(SpO2)12 - Label set 3201274-015 Front connector label, E

(no SpO2)12 - Label set 3201275 Physio-Control logo lab12 - Label set 3201273 Product ID label12 - Label set 3009060 FDA label 12 - Label set 3202375 Masimo patent label23 3201499 Manual latch label 183 3201643 Serial number label284 3206926-001 Label - Adult VF Dose,



F

LaDi

tion.

2-A12-B

12-C

12-DFront view

(No SpO2)

284

A15

9-153



inal Assembly (continued)

bel Placement agrams

Refer to the parts list for label descrip

12-E

183

12-F

1

Bottom view Rear view



F

LIDeLa

Part Description

804 LIFEPAK 20 label set (no SpO2)

818 LIFEPAK 20 label set (with SpO2)

754 LIFEPAK 20e label set (no SpO2)

755 LIFEPAK 20e label set (with SpO2)

660 LIFEPAK 20e label set (no SpO2) 3rd Edition

661 LIFEPAK 20e label set (with SpO2) 3rd Edition





666 LIFEPAK 20e label set (no SpO2)3rd Edition

667 LIFEPAK 20e label set (with SpO2)3rd Edition


9-154




FEPAK 20/20e vice Label Set nguages

Language MIN CAT.

English 3201640-500 21501-001

English 3201640-501 21501-001

English 3206034-006 21501-001

English 3206034-007 21501-001

English 3206034-008 21501-002

English 3206034-009 21501-002

French 3201640-506 21501-001

French 3201640-507 21501-001

French 3206034-084 21501-001

French 3206034-085 21501-001

French 3206034-086 21501-002

French 3206034-087 21501-002



F

LIDeLa

Part Description













9-155




FEPAK 20/20e vice Label Set nguages (continued)

Language MIN CAT.

German 3201640-502 21501-001

German 3201640-503 21501-001

German 3206034-044 21501-001

German 3206034-045 21501-001

German 3206034-046 21501-002

German 3206034-047 21501-002

Spanish 3201640-510 21501-001

Spanish 3201640-511 21501-001

Spanish 3206034-128 21501-001

Spanish 3206034-129 21501-001

Spanish 3206034-126 21501-002

Spanish 3206034-127 21501-002



F

LIDeLa

Part Description














9-156





Language MIN CAT.

Italian 3201640-504 21501-001

Italian 3201640-505 21501-001

Italian 3206034-064 21501-001

Italian 3206034-065 21501-001

Italian 3206034-066 21501-002

Italian 3206034-067 21501-002

Swedish 3201640-516 21501-001

Swedish 3201640-517 21501-001

Swedish 3206034-184 21501-001

Swedish 3206034-185 21501-001

Swedish 3206034-186 21501-002

Swedish 3206034-187 21501-002



F

LIDeLa

Part Description













9-157





Language MIN CAT.

Danish 3201640-518 21501-0018

Danish 3201640-519 21501-0018

Danish 3206034-204 21501-0017

Danish 3206034-205 21501-0017

Danish 3206034-206 21501-0026

Danish 3206034-207 21501-0026

Dutch 3201640-508 21501-0018

Dutch 3201640-509 21501-0018

Dutch 3206034-104 21501-0017

Dutch 3206034-105 21501-0017

Dutch 3206034-106 21501-0026

Dutch 3206034-107 21501-0026



F

LIDeLa

Part Description














9-158





Language MIN CAT.

Finnish 3201640-520 21501-001

Finnish 3201640-521 21501-001

Finnish 3206034-224 21501-001

Finnish 3206034-225 21501-001

Finnish 3206034-226 21501-002

Finnish 3206034-227 21501-002

Norwegian 3201640-522 21501-001

Norwegian 3201640-523 21501-001

Norwegian 3206034-244 21501-001

Norwegian 3206034-245 21501-001

Norwegian 3206034-246 21501-002

Norwegian 3206034-247 21501-002



F

LIDeLa

Part Description














9-159





Language MIN CAT.

Polish 3201640-524 21501-0018

Polish 3201640-525 21501-0018

Polish 3206034-264 21501-0017

Polish 3206034-265 21501-0017

Polish 3206034-266 21501-0026

Polish 3206034-267 21501-0026

Portuguese 3201640-512 21501-0018

Portuguese 3201640-513 21501-0018

Portuguese 3206034-144 21501-0017

Portuguese 3206034-145 21501-0017

Portuguese 3206034-146 21501-0026

Portuguese 3206034-147 21501-0026



F

LIDeLa

Part Description













9-160





Language MIN CAT.

Brazilian 3201640-514 21501-0018

Brazilian 3201640-515 21501-0018

Brazilian 3206034-164 21501-0017

Brazilian 3206034-165 21501-0017

Brazilian 3206034-166 21501-0026

Brazilian 3206034-167 21501-0026

Japanese 3201640-536 21501-0009

Japanese 3201640-537 21501-0009

Japanese 3206034-404 21501-0017

Japanese 3206034-405 21501-0017

Japanese 3206034-406 21501-0026

Japanese 3206034-407 21501-0026



F

LIDeLa

Part Description













9-161





Language MIN CAT.

Chinese 3201640-532 21501-0018

Chinese 3201640-533 21501-0018

Chinese 3206034-344 21501-0015

Chinese 3206034-345 21501-0015

Chinese 3206034-346 21501-0026

Chinese 3206034-347 21501-0026

Hungarian 3201640-526 21501-0018

Hungarian 3201640-527 21501-0018

Hungarian 3206034-284 21501-0017

Hungarian 3206034-285 21501-0017

Hungarian 3206034-286 21501-0026

Hungarian 3206034-287 21501-0026



F

LIDeLa


Part Description













9-162





Language MIN CAT.

Czech 3201640-528 21501-0018

Czech 3201640-529 21501-0018

Czech 3206034-304 21501-0017

Czech 3206034-305 21501-0017

Czech 3206034-306 21501-0026

Czech 3206034-307 21501-0026

Russian 3201640-530 21501-0018

Russian 3201640-531 21501-0018

Russian 3206034-324 21501-0017

Russian 3206034-325 21501-0017

Russian 3206034-326 21501-0026

Russian 3206034-327 21501-0026



F

LIDeLa

Part Description







9-163





Language MIN CAT.

Korean 3201640-534 21501-0018

Korean 3201640-535 21501-0018

Korean 3206034-384 21501-0015

Korean 3206034-385 21501-0015

Korean 3206034-386 21501-0026

Korean 3206034-387 21501-0026



F

MLa

NlatoD

-000767

-000924

-000925

-000767

-000932

-000925

-000924

-000930

-000929

-000925

-000928


9-164




anual Latch Labelnguages

ote: To order the MANUAL tch label and the AED door gether as a kit refer to AED oor/Latch Label Kits.

Language MIN CAT.

English 3201499-900 21501

French 3201499-902 21501

German 3201499-901 21501

Spanish 3201499-900 21501

Italian 3201499-060 21501

Swedish 3201499-901 21501

Danish 3201499-902 21501

Dutch 3201499-100 21501

Finnish 3201499-220 21501

Norwegian 3201499-901 21501

Polish 3201499-260 21501



F

MLa

NlatoM

1-000767

1-000767

1-000926

1-000927

1-001349

1-001350

1-001351

1-001352

9-165




anual Latch Labelnguages (continued)

ote: To order the MANUAL tch label and the AED door gether as a kit refer to anual Latch Label Kits.

Language MIN CAT.

Portuguese 3201499-900 2150

Brazilian 3201499-900 2150

Japanese 3201499-400 2150

Chinese 3201499-340 2150

Hungarian 3201499-280 2150

Czech 3201499-300 2150

Russian 3201499-320 2150

Korean 3201499-380 2150



FAdLa

Sedi

01935

01858

01856

01860

01857

01862

01863

01859

01864

01865

01866

01861

01867

01868

01869

01870

01871

01872

9-166




ult VF Dose Labelnguages (284)

e Labels Assembly agram

Language MIN CAT.English 3206926-001 21501-0

French 3206926-081 21501-0

German 3206926-041 21501-0

Spanish 3206926-121 21501-0

Italian 3206926-061 21501-0

Swedish 3206926-181 21501-0

Danish 3206926-201 21501-0

Dutch 3206926-101 21501-0

Finnish 3206926-221 21501-0

Norwegian 3206926-241 21501-0

Polish 3206926-261 21501-0

Portuguese 3206926-141 21501-0

Hungarian 3206926-281 21501-0

Czech 3206926-301 21501-0

Russian 3206926-321 21501-0

Chinese 3206926-341 21501-0

Korean 3206926-380 21501-0

Japanese 3206926-401 21501-0



F

AEKi

K iption

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

3 202056) and Latch label (3201499)

9-167




D Door/Latch Labelts

it MIN CAT. Languages Part Descr

202360-027 21330-001007 English, Spanish, Portuguese, Brazilian

AED door (3

202360-028 21330-001008 German, Swedish, Norwegian

AED door (3

202360-029 21330-001009 Italian AED door (3

202360-030 21330-001010 French, Danish AED door (3

202360-031 21330-001011 Dutch AED door (3

202360-032 21330-001012 Finnish AED door (3

202360-033 21330-001013 Polish AED door (3

202360-034 21330-001014 Chinese AED door (3

202360-035 21330-001015 Japanese AED door (3



F

A1Ke

e for language MINs.)


9-168




5 Elastomer ypad – All Options

(Refer to the parts list on the next pag



F

A1Ke

. Part Description

00-004598 Keypad (no Pacing)

00-004231 Keypad (with Pacing)












9-169




5 Elastomer ypad - Languages

Language MIN CAT

English 3200642-106 213

English 3200642-091 213

French 3200642-107 213

French 3200642-092 213

German 3200642-108 213

German 3200642-093 213

Spanish 3200642-109 213

Spanish 3200642-094 213

Italian 3200642-110 213

Italian 3200642-095 213

Swedish 3200642-111 213

Swedish 3200642-096 213



F

A1Ke(c

. Part Description














9-170





ontinued)

Language MIN CAT

Danish 3200642-112 2130

Danish 3200642-097 2130

Dutch 3200642-113 2130

Dutch 3200642-098 2130

Finnish 3200642-114 2130

Finnish 3200642-099 2130

Norwegian 3200642-115 2130

Norwegian 3200642-100 2130

Polish 3200642-116 2130

Polish 3200642-101 2130

Portuguese 3200642-117 2130

Portuguese 3200642-102 2130



F

A1Ke(c

. Part Description















9-171





ontinued)Language MIN CAT

Brazilian 3200642-118 2130

Brazilian 3200642-103 2130

Japanese 3200642-141 2130

Japanese 3200642-140 2130

Chinese 3200642-123 2130

Chinese 3200642-122 2130

Hungarian 3200642-126 2130

Hungarian 3200642-125 2130

Czech 3200642-129 2130

Czech 3200642-128 2130

Russian 3200642-132 2130

Russian 3200642-131 2130

Korean 3200642-135 2130

Korean 3200642-134 2130



F

In o the printer: the left side of the device to open the

aper chamber, with the end coming from

perly if the paper roll is inserted with the . The paper roll must be inserted with the

the paper end extends out of the side of

9-172




stalling Printer Paper To install a new roll of printer paper int1. Press the printer button located on

printer door.2. Remove the old roll of paper.3. Insert the new paper roll into the p

under the roll.Note: The printer will not print proend coming over the top of the rollend coming from under the roll.

4. Close the printer door. Ensure thatthe printer.



F

StLa

215

1

Asse guages Charge Button Languages

9-173




andard Paddles bels and Buttons 215

211

213 2x

Apex paddle

Sternum paddle

mbly Diagrams Parts 1–17 Parts 19–215 Label Lan



F

StPa


Lab l Languages Charge Button Languages

It Note

29 r

21 Refer to Charge Button Languages

21

21 Refer to Standard Paddles Label Languages

9-174





andard Paddles rts List

els and Buttons Assembly Diagrams Parts 19–215 Labe

em Quantity MIN CAT. Part Description

2 3200941-003 21330-001024 Standard paddle adapteassembly

1 1 3200648 various Charge button

3 2 3200943-000 21300-004710 Shock button

5 2 3202523 21501-000997 Paddle label



F

StLa

T.

01-000823

01-000823

01-000823

01-000824

01-000827

01-000823

01-000823

01-000823

01-000828

01-000823

01-000829


Lab rts 19–215 Charge Button Languages

9-175





andard Paddles Label nguages

Language MIN CA

English 3202533-000 215

French 3202533-000 215

German 3202533-000 215

Spanish 3202533-001 215

Italian 3202533-002 215

Swedish 3202533-000 215

Danish 3202533-000 215

Dutch 3202533-000 215

Finnish 3202533-003 215

Norwegian 3202533-000 215

Polish 3202533-004 215

els and Buttons Assembly Diagrams Parts 1–17 Pa



F

StLa

T.

501-000809

501-000809

501-000823

501-000807

501-001428

501-001429

501-001430

501-001431

Lab rts 19–215 Charge Button Languages

9-176




andard Paddles Label nguages (continued)

Language MIN CA

Portuguese 3202533-005 21

Brazilian 3202533-005 21

Japanese 3202533-000 21

Chinese 3202533-006 21

Hungarian 3202533-280 21

Czech 3202533-300 21

Russian 3202533-320 21

Korean 3202533-380 21




F

ChLa

-004886

-004756

-004766

-004757

-004758

-004759

-004760

-004766

-004761

-004762

-004763


Lab rts 19–215 Label Languages

9-177




arge Button nguages

Language MIN CAT.

English 3200648-015 21300

French 3200648-016 21300

German 3200648-902 21300

Spanish 3200648-017 21300

Italian 3200648-018 21300

Swedish 3200648-019 21300

Danish 3200648-020 21300

Dutch 3200648-902 21300

Finnish 3200648-021 21300

Norwegian 3200648-022 21300

Polish 3200648-023 21300




F

ChLa

.

00-004767

00-004767

00-004764

00-004765

00-006328

00-006329

00-006330

00-006331

Lab rts 19–215 Label Languages

9-178




arge Button nguages (continued)

Language MIN CAT

Portuguese 3200648-903 213

Brazilian 3200648-903 213

Japanese 3200648-024 213

Chinese 3200648-025 213

Hungarian 3200648-280 213

Czech 3200648-300 213

Russian 3200648-320 213

Korean 3200648-380 213




S

omponents that support a particular

rt Description

-REPAIR, TOP CASE HANDLE

-REPAIR, FRONT CASE

REPAIR, DISPLAY FOR UI 3201966-005 D -006 (Pre-Redux)

REPAIR, BACKLIGHT INVERTER FOR UI 01966-005 AND -006 (Pre-Redux)

-REPAIR, POWER MODULE, LIFEPAK 20

-REPAIR, MASIMO SPO2 CONNECTOR

-REPAIR, THERAPY PCBA, PACING

-REPAIR, THERAPY PCBA, PACING


9-179



ervice Replacement Kits

The service replacement kits include creplacement activity.

Kit MIN CAT. Pa

3202718-000 40402-000001 KIT

3202718-001 40402-000002 KIT

3202718-008 40402-000009 KITAN

3202718-009 40402-000010 KIT32

3202718-010 40402-000011 KIT

3202718-013 40402-000014 KIT

3202718-035 (RoHS)

40402-000028 KIT

3202718-016 (non-RoHS)

40402-000003 KIT



Srt Description

-REPAIR, THERAPY PCBA, NON PACING

-REPAIR, THERAPY PCBA, NON PACING

-REPAIR, OEM PCBA

-REPAIR, OEM PCBA

-REPAIR, PATIENT PARAMETER PCBA

-REPAIR, PATIENT PARAMETER PCBA

-REPAIR, PCB STACK

9-180




ervice Replacement Kits (continued)

Kit MIN CAT. Pa

3202718-036 (RoHS)

40402-000029 KIT

3202718-017 (non-RoHS)

40402-000004 KIT

3202718-037 (RoHS)

40402-000030 KIT

3202718-019 (non-RoHS)

40402-000006 KIT

3202718-038 (RoHS)

40402-000031 KIT

3202718-020 (non-RoHS)

40402-000007 KIT

3202718-021 40402-000017 KIT



S

art Description

IT-REPAIR, POWER MODULE, LIFEPAK 20e

IT-REPAIR, POWER MODULE, LIFEPAK 20e

IT-REPAIR, CAPACITOR BRACKET

IT-REPAIR, CAPACITOR,

IT-REPAIR, THERAPY CONNECTOR

IT-REPAIR, THERAPY CONNECTOR

IT-REPAIR, REDUX SC PCBA AND UI PCBA

IT-REPAIR, REDUX SC PCBA AND UI PCBA

9-181





Kit MIN CAT. P

3202718-039 (RoHS)

40402-000032 K

3202718-022 (non-RoHS)

40402-000018 K

3202718-024 40402-000020 K

3202718-025 40402-000021 K

3202718-043 (RoHS)

40402-000036 K

3202718-026 (non-RoHS)

40402-000022 K

3202718-040 (RoHS)

40402-000033 K

3202718-029 (non-RoHS)

40402-000025 K



Sart Description

IT-REPAIR, SPO2 MODULE

IT-REPAIR, SPO2 MODULE

IT-REPAIR, MNC FLASH SPO2, IFEPAK 20e

IT-REPAIR, MNC FLASH SPO2, LIFEPAK 20e

IT-REPAIR, LED DISPLAY FOR Redux UI317230-000 (RoHS), Post-Redux UI 3317230-02 (RoHS) and 3201966-007 (non-RoHS) - LED isplay and Backlight for Redux UI PCB 317230-000 (RoHS), Post-Redux UI 3317230-02 (RoHS) or 3201966-007 (non-RoHS) or reater (requires Redux level PCB software set)

IT-REPAIR, Post Redux, UI, SC, Printer, RoHS

IT-REPAIR, Post Redux, UI, Printer, RoHS

9-182




Kit MIN CAT. P

3202718-041 (RoHS)

40402-000034 K

3202718-030 (non-RoHS)

40402-000026 K

3202718-042 (RoHS)

40402-000035 KL

3202718-031 (non-RoHS)

40402-000019 K

3202718-032 40402-000027 K30D30g

3202718-044 40402-000037 K

3202718-045 40402-000038 K



SIT-REPAIR, Post Redux, UI, RoHS

IT-REPAIR, Post Redux SC, RoHS

IT-REPAIR, Post Redux, Printer, RoHS

9-183




3202718-046 40402-000039 K

3202718-047 40402-000040 K

3202718-048 40402-000041 K



S

KITHAM

KITM

. Part Description

Top case handle

00-005334 Machine screw 6-32 x 1.75L

00-001032 Machine screw 6-32x0.375L

. Part Description

Front case, pad printed

00-004837 Cover plate, door

00-004836 Door hinge plate

00-004233 Display lens

00-005334 Machine screw 6-32 x 1.75L

00-001032 Machine screw 6-32x0.375L

9-184




-REPAIR, TOP CASE NDLEIN 3202718-000

-REPAIR, FRONT CASEIN 3202718-001

Item Quantity MIN CAT

2 1 3200631

167 2 202253-592 213

169 2 3206185-001 213


9 1 3200624

19 1 3200638-001 213

37 1 3200637-001 213

43 1 3200913-003 213

167 4 202253-592 213

169 2 3206185-001 213



S

KITUI (PrM

KITINV00M

T. Part Description

Active Color LCD Display

300-007774 Active Display Cable


300-001038 Screws 4-40 x 0.312

300-006141 Nylon snap rivet

T. Part Description

Backlight Inverter

00-004237 Active Backlight Inverter Cable

00-004838 Active Display Bracket

00-004250 Extender cable (for Sanyo display devices)

9-185




-REPAIR, DISPLAY FOR 3201966-005 AND -006 e-Redux)IN 3202718-008

-REPAIR, BACKLIGHT ERTER FOR UI 3201966-

5 AND -006 (Pre-Redux)IN 3202718-009

Item Quantity MIN CA

A11 1 3205278-001

W15 1 3300152-000 21

43 1 3200913-003 21

173 4 202253-761 21

266 1 3205497-308 21


A08 1 3202033-500

W17 1 3200996-002 213

47 1 3200640-015 213

203 1 3202018-000 213



S

KITMOM

KITCOM

KITPAM(R32(n

T. Part Description

Power Supply module

T. Part Description

SpO2 Flex Assembly

SpO2 connector mounting clip

AT. Part Description

Therapy PCB with pacing

Therapy PCB with pacing

300-4242

ISO mount, Therapy

9-186




-REPAIR, POWER DULE, LIFEPAK 20

IN 3202718-010

-REPAIR, MASIMO SPO2 NNECTOR

IN 3202718-013

-REPAIR THERAPY PCB, CINGIN 3202718-035 oHS) or 02718-016 on-RoHS)


A03 1 3202131-010


W05 1 3200925-006

113 1 3200921-000

Item Quantity MIN C

A04 1 3317228-000 (RoHS)

A04 1 3202259-010 (non-RoHS)

123 5 3201374-010 2100



S

KITWIM(R32(n

KITM(R32(n

T. Part Description

Therapy PCB without pacing

Therapy PCB without pacing

300-004242 ISO mount, Therapy

T. Part Description

OEM Interface PCB

OEM Interface PCB

00-008019 Machine screw, SEMS 4-40 x 5/16 L, split washer

00-005120 Screw-Cap, Hex,4-40 x 0.312 Nylon

9-187




-REPAIR THERAPY PCB, THOUT PACINGIN 3202718-036 oHS) or 02718-017 on-RoHS)

-REPAIR, OEM PCBAIN 3202718-037 oHS) or 02718-019 on-RoHS)


A04 1 3317228-001 (RoHS)

A04 1 3202259-011 (non-RoHS)

123 5 3201374-010 21


A06 1 3317224-000 (RoHS)

A06 1 3201950-004 (non-RoHS)

252 1 201874-002 213

255 1 3202489-031 213



S

KITPAM(R32(n

T. Part Description

Patient Parameter PCB

30-001266 Patient Parameter PCB

00-006430 Screw 4-40 1.000L

9-188




-REPAIR, PATIENT RAMETER PCBAIN 3202718-038 oHS) or 02718-020 on-RoHS)


A06 1 3317226-000 (RoHS)

A06 1 3202680-002 (non-RoHS)

213

125 1 202253-772 213



S

KITM

T. Part Description

00-006430 Screw 4-40 1.000L

00-004236 Boardstack shield

00-004815 Standoff-M/M 0.250 hex, 0.375

00-004243 ISO mount, OEM

00-001038 Screw, 4-40 x 0.312L

00-008019 Machine screw SEMS 4-40 x 5/16 L, split washer

00-005187 ISO mount, Parameter

00-006038 Nomex shield

00-000580 Washer, 0.125ID, 0.312D

00-006593 Shield - EMI, PCB Stack

9-189




-REPAIR, PCB STACKIN 3202718-021


125 1 202253-772 213

127 1 3200927-006 213

129 5 3201375-006 213

149 3 3201374-011 213

173 2 202253-761 213

252 5 201874-002 213

258 1 3201374-012 213

262 1 3203897-000 213

264 2 200804-102 213

278 1 3206405-000 213



S

KITMOM(R32(n

. Part Description

Power Supply module

Power Supply module

Battery Cable LIFEPAK 20e

Power/Therapy Cable, LIFEPAK 20e

ECG Sync/System Cables

AC Power Cable, LIFEPAK 20e

9-190




-REPAIR, POWER DULE, LIFEPAK 20e

IN 3202718-039 oHS) or 02718-022 on-RoHS)


A03 1 3317740-000 (RoHS)

A03 1 3202131-009 (non-RoHS)

W08 1 3206579

W10 1 3206857

W11 1 3201997

W13 1 3206469



S

KITBRM

. Part Description

00-004619 Capacitor Support Bracket

00-001038 Screw, 4-40 x 0.312L

00-006962 Dielectric shield

00-003883 Standoff, 0.188 hex, 0.562L

9-191




-REPAIR, CAPACITOR ACKETIN 3202718-024


95 2 3200922-000 213

173 4 202253-761 213

238 1 3206900-001 213

22 2 3202228-562 213



S

KITM T. Part Description

Energy Storage Capacitor

00-004307 Capacitor Discharge Cable

00-007458 Foam spacer

00-004110 Capacitor dielectric shield

00-000499 Cable tie retainer

00-004807 Foam, Capacitor end

00-005068 Inductive Resistor Assy.

00-004619 Capacitor bracket support

00-001038 Screw, 4-40 x 0.312L

00-003883 Standoff, 0.188 hex,0.562L

00-006962 Dielectric shield

00-007794 Poron Foam, Capacitor

9-192




-REPAIR, CAPACITORIN 3202718-025 Item Quantity MIN CA

A13 1 3200846

W07 1 3202383-001 213

93 2 804447-36 213

162 1 3009787-003 213

229 1 200536-001 213

240 1 804447-041 213

260 1 3202773-000 213

95 2 3200922-000 213

173 4 202253-761 213

22 2 3202228-562 213

238 1 3206900-001 213

241 1 3300694-000 213



S

KITCOM(R32(n

. Part Description

Therapy Connector Assembly

Therapy Connector Assembly

00-000149 Therapy retaining ring

00-005784 Seal, therapy connector

9-193




-REPAIR, THERAPY NNECTOR

IN 3202718-043 oHS) or 02718-026 on-RoHS)


W01 1 3200474-009 (RoHS)

W01 1 3200474-008 (non-RoHS)

111 1 200040-001 213

268 1 3203445-001 213



S

KITPCM(R32(n

. Part Description

System Controller PCB

System Controller PCB

User Interface PCB

User Interface PCB


00-006430 Screw 4-40 1.000L

00-004236 Boardstack shield

00-004815 Standoff-M/M 0.250 hex, 0.375


9-194




-REPAIR, REDUX SC BA AND UI PCBAIN 3202718-040 oHS) or 02718-029 on-RoHS)


A01 1 3317227-002(RoHS)

A01 1 3201964-015 (non-RoHS)

A05 1 3317230-000 (RoHS)

A05 1 3201966-007 (non-RoHS)

W15 1 3300152-000 213

125 2 202253-772 213

127 1 3200927-006 213

129 5 3201375-006 213



S

KITPCM(R32(n

. Part Description

00-004704 Boardstack connector

00-004243 ISO mount, OEM

00-001038 Screws 4-40 x 0.312

00-004807 Spacer Foam, UI PCB


00-005187 ISO mount, Parameter

00-006038 Nomex shield

00-000580 Washer, 0.125ID, 0.312D

00-005578 ISO mount, System Controller (standoff)

00-006593 Shield - EMI, PCB Stack

9-195




-REPAIR, REDUX SC BA AND UI PCBAIN 3202718-040 oHS) or 02718-029 on-RoHS) (continued)


135 1 3201007-002 213

149 3 3201374-011 213

173 2 202253-761 213

240 1 804447-041 213

252 5 201874-002 213

258 1 3201374-012 213

262 1 3203897-000 213

264 2 200804-102 213

265 1 3201374-009 213

278 1 3206405-000 213



S

KITM(R32(n

. Part Description

OEM Module, Pulse Oximeter, 3336

OEM Module, Pulse Oximeter, 3336




9-196




-REPAIR, SPO2 MODULE IN 3202718-041 oHS) or 02718-030 on-RoHS)


A10 1 3318279 (RoHS)

A10 1 3308709 (non-RoHS)

W03 1 3200926-007 (RoHS)

213

W03 1 3200926-006 (non-RoHS)

213

252 4 201874-002 213



S

KITSPM(R32(n

T. Part Description

OEM Module, Pulse Oximeter, 3336 (MNC programmed)

OEM Module, Pulse Oximeter, 3336 (MNC programmed)




Software-Dual Flash, MNC MasimoSoftware-Dual Flash, MNC Masimo

9-197




-REPAIR, MNC FLASH O2, LIFEPAK 20e (Nellcor)IN 3202718-042 oHS) or 02718-031 on-RoHS)


A10 1 3318279 (RoHS)

A10 1 3308709 (non-RoHS)

W03 1 3200926-007 (RoHS)

213

W03 1 3200926-006 (non-RoHS)

213

252 4 201874-002 213

0 0 3319549-000 (RoHS)

0 0 3207319-100 (non-RoHS)



S

KITFOan- Lfor0000(rePCMI

T. Part Description

Module-OEM, LED Driver (Backlight Inverter)

Active Display, Color LED



00-004838 Active Display Bracket

00-001038 Screws 4-40 x 0.312

00-006141 Nylon snap rivet

9-198




-REPAIR, LED DISPLAY R UI 3317230-000 (RoHS) d 3201966-007 (non-RoHS) ED Display and Backlight Redux UI PCB 3317230-0 (RoHS) or 3201966-7(non-RoHS) or greater quires Redux level Bsoftware set)

N 3202718-032


A08 1 3308907

A11 1 3309555

W15 1 3300152-000 213

43 1 3200913-003 213

47 1 3200640-015 213

173 4 202253-761 213

266 1 3205497-308 213



S

KITUI,M

T. Part Description

Washer, Flat, Round, S, Zinc, 0.312D, 0.125ID

Screw-M, PH, CP, P, Sems, #4-40, 5-16 L, Split Washer

Screw-M, CS, Z, PH, Nylock, 4-40 X 1.000

Screw, Machine, Panead, Nylok, 4-40 X 1.000

Shield - PCB Stack

Connector-Board Stacker, Modified

Mount-Isolation, PCB, System Controller

Mount-Isolation, PCB, OEM

9-199




- REPAIR, POST REDUX SC, PRINTER, ROHSIN 3202718-044


2 200804-102

1 201874-002

16 202253-761

1 202253-772

1 3200927-006

1 3201007-002

1 3201374-009

3 3201374-011



S

KITUI,(coM

T. Part Description

Mount-Isolation, PCB, Parameter

Standoff - Male/Male, 0.250 HEX, 0.375L

Shield - Nomex

Shield - EMI, PCB Stack

Cable - Assembly, Active Color, RoHS

Screw, Machine, Panhead, Nylok, 6-32 X 1.750

Screw-PH, SS, P, Nylok, 6-32 X 0.375

Flex Assembly - UI To Stack

Screw-Cap, SKT HD, Hex Rec, 4-40, 0.312L, NYL

9-200




- REPAIR, POST REDUX SC, PRINTER, ROHS ntinued)IN 3202718-044


1 3201374-012

5 3201375-006

1 3203897-000

1 3206405-000

1 3300152-000

4 202253-592

2 3206185-001

1 3201000-004

2 3202489-031



S

KITUI,(coM

T. Part Description

Nut-Hex, SS, Lock 4-40 X 0.250W

Spacer-Foam, LP20 UI PCB

PCB Assy-Programmed System Controller, LP20

PCB Assy-Programmed User Interface, LP20

Printer-50MM, Thermal Printhead, RoHS

9-201




- REPAIR, POST REDUX SC, PRINTER, ROHS ntinued)IN 3202718-044


9 200805-000

1 80447-041

1 3317227-002

1 3317230-002

1 3318747-001



S

KITUI,M

T. Part Description

Screw-M, CS, Z, PH, Nylock, 4-40 X 0.312L

Cable-Assembly, Active Color, RoHS




PCB Assy - Programmed User Interface, LP20


9-202




- REPAIR, POST REDUX PRINTER, ROHSIN 3202718-045


13 3202718-045

1 3300152-000

3 200805-000

4 202253-592

2 3206185-001

1 3317230-002

1 3318747-001



S

KITUI,M

T. Part Description


Cable-Assembly, Active Color, RoHS




PCB Assy - Programmed User Interface, LP20


9-203




- REPAIR, POST REDUX ROHSIN 3202718-046


13 202253-761

1 3300152-000

3 200805-000

4 202253-592

2 3206185-001

1 3317230-002

1 3318747-001



S

KITSCM

T. Part Description

Washer, Flat, Round, S, Zinc, 0.312D, 0.125ID

Screw-M, PH, SP, P, Sems, # 4-40, 5-16 L, Split Washer



Connector-board Stacker, Modified

Standoff - Male/Male, 0.250 Hex, 0.375L

Shield - Nomex


9-204




- REPAIR, POST REDUX , ROHS IN 3202718-047


2 200804-102

1 201874-002

5 202253-761

1 202253-772

1 3201007-002

5 3201375-006

1 3203897-000

4 202253-592



S

KITSCM

T. Part Description



SCREW-CAP, SKT HD, HEX REC, 4-40, 0.312L, NYL

PCB Assy-Programmed System Controller, LP20

9-205




- REPAIR, POST REDUX , ROHS (continued)IN 3202718-047


2 3206185-001

6 200805-000

2 3202489-031

1 3317227-002



S

KITPRM

T. Part Description


9-206




- REPAIR, POST REDUX, INTER, ROHS IN 3202718-048


1 3318747-001



D

em software replacement require tools Physio-Control. These procedures and mers using LIFENET System Asset ration and software can also be installed ersonnel.

rvices representative for assistance.

9-207



evice Software Replacement

Device configuration settings and systand procedures that are proprietary totools may be available for use by custoManagement products. Device configuby authorized Physio-Control service pContact a Physio-Control customer se

P Table of Contents Section Contents Back Index Next Page

LIF Defibrillator/Monitor Replacement Procedures

D Number and Serial Number

PN el The device serial number (SN) and part number (PN) are noted on a label on the bottom of the device.

9-208

01643-020K 20 2nd Edition

Conforms to medical device directive93/42/EEC

Splash proof per IEC 60529

Operating voltageAC line frequency

Power consumption Volt-Amperes

8-digit serial number

10-digit part number

Year of manufacture

CSA certification for Canada and the United States

Do not dispose in unsorted waste stream 11-digit catalog

number

Chinese environmentally friendly use period

Consult operating instructions

3201643-025LIFEPAK 20e 2nd Edition

revious Page

EPAK 20/20e

evice Part

and SN Lab

32LIFEPA

P Table of Contents Section Contents Back Index Next Page

LIF Defibrillator/Monitor Replacement Procedures

D Number and Serial Number (continued)

PN l The device serial number (SN) and part number (PN) are noted on a label on the bottom of the device.

9-209

01643-021 20 no CE Mark

3201643-026LIFEPAK 20e no CE Mark

revious Page

EPAK 20/20e

evice Part

and SN Labe

32LIFEPAK



D ntinued)

t number (PN) are noted on a label on the

9-210

PN

3201643-030LIFEPAK 20e 3rd Edition,

no CE Mark



evice Part Number and Serial Number (co

The device serial number (SN) and parbottom of the device. and SN Label

3201643-029LIFEPAK 20e 3rd Edition



D tinued)

UnNu

3202487-072, reflects the device options, nd so forth.

UnSe

ted to the sales order created during the serial number label on the bottom of ing to order parts.

9-211



evice Part Number and Serial Number (con

derstanding the Part mber

The device part number, for example, features, language, operating power, a

derstanding the rial Number

The serial number for the device is reladevice manufacturing and appears on the device. Use this number when call



O

io-Control representative. In the USA, call er and serial number located on the bly numbers, MINs (part numbers),

ns. Parts may be substituted to reflect s.

M u may also need the device g date is available for viewing by

Se ies the manufacturing conditions and e. When ordering parts, use the serial bottom of the device.

9-212



rdering Parts

To order parts, contact your local Phys1.800.442.1142. Provide the part numbbottom of the device. Specify all assemreference designations, and descriptiodevice modifications and improvement

anufacturing Date In some cases when ordering parts, yomanufacturing date. This manufacturinaccessing the Device Log.

rial Number The serial number of the device identifelements used in producing your devicnumber (SN) listed on the label on the



LIS

n the Operating Instructions for the device. in this section.



3FEPAK 20/20e pecifications

Detailed specifications are provided iAdditional specifications are included


LIF LIFEPAK 20/20e Specifications

G

Op 68°F) unless otherwise stated.itor has seven main operating modes:erating capability for ALS userserating capability for BLS usersrint, edit or delete previous patient

onfigure the instrumentxecute device diagnostic tests and

waveforms for demonstration purposesmatic tests of critical circuits

10-2



eneral

eration Modes Note: All specifications are at 20°C (The LIFEPAK 20/20e defibrillator/monManual Mode - Provides normal opAED Mode - Provides normal opArchive Mode - Allows operator to p

recordsSetup Mode - Allows operator to cService Mode - Allows operator to e

calibrationsInservice Mode - Provides simulatedAuto Test Mode - Provides daily auto

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LIFEPAK 20 LIFEPAK 20e - Stryker CorporationQUIK-COMBO® pacing/defibrillation/ECG elec trodes —...

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