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Page 1: L3_QG_5122541_4_100

GE Healthcare

TechnicalPublications

Direction 5122541-100Rev. 4

LOGIQ 3 Ex

Quick Guide

Copyright©2005, 2006

Operating Documenta

pert/LOGIQ 3 Pro/LOGIQ 3

,2010 By General Electric Co.

tion

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GE Healthcare

GE Medical System: Telex 3797371P. O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.(Asia, Pacific, Latin America, North America)

GE Ultraschall TEL: 49 212.28.02.207Deutschland GmbH & Co. KG FAX: 49 212.28.02.431Beethovenstraße 239Postfach 11 05 60D-42655 Solingen GERMANY

Regulatory Requirement

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LOGI A

REV1

2

3

4

N FOR CHANGEease

graphics

anged on the manual

CE Marking

aintained on GPC (GE Medical Sales Representative or in the

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Revision History

DATE18 Feb, 2005

11 Jan, 2006

24 Apr, 2006

15 Mar 2010

REASOInitial Rel

Updated

Label Ch

Removed

List of Effective Page

PAGE REVISIONNUMBER HISTORY

Title Rev. 4A and B Rev. 4

1-54 Rev. 4

Please verify that you are using the latest revision of this document. Information pertaining to this document is mSystems Global Product Configuration). If you need to know the latest revision, contact your distributor, local GEUSA call the GE Ultrasound Clinical Answer Center at 1-800-682-5327 or 262-524-5698.

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LOGI B

e United States.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

CAUTION FOR USA ONLY

“United Sates law restricts this device to sale or use by or on the order of a physician” if sold in th

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LOGI 1

Pre

Syste

Powe

To con

1. Enam23

2. En

Power switch to turn the power on. The aker must also be in the on position.

-3. Power On/Standby Switch Location

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

paring for an Exam

m Power

r On

nect the system to the electrical supply:

sure that the wall outlet is a minimum 10 p dedicated circuit for 110VAC/115VAC/0VAC

Figure 1-1. Example Plug and Outlet Configurations

a. 100-120 VAC, 1250VAPlug and Outlet Configuration(USA)

b. 220-240 VAC, 1250VAPlug and Outlet Configuration (Europe)

sure that the power switch is turned off.

3. Unwrap the power cable. Make sure to allow sufficient slack in the cable so that the plug is not pulled out of the wall if the system is moved slightly.

4. Attach the power plug to the system and secure it in place by using the retaining clamp.

Figure 1-2. Power Plug

a. Retaining clamp for power plug

CAUTION: Ensure that the retaining clamp for the power plug is fixed firmly.

Use caution to ensure that the power cable does not disconnect during system use. If the system is accidentally unplugged, data may be lost.

Press thecircuit bre

Figure 1

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LOGI 2

Powe

To pow

1. Prfro

2. Th

3. UsShThanillu

4. DiClStoda

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

r Off

er down the system:

ess the Power On/Standby switch at the nt of the system once.e System-Exit window is displayed.

ing the Trackball or Tab key, select utdown.e shutdown process takes a few seconds d is completed when the control panel mination is turned off.

sconnect the probes.ean or disinfect all probes as necessary. re them in their shipping cases to avoid

mage.

Starting an Exam

You need to select a pre-configured dataflow that sets up the ultrasound system to work according to the services associated to the dataflow.

1. Select your Operator Login and type in your Password:

2. Press OK. 3. Fill in the New Patient menu as described on

Page 3.

OR,If the patient name is on the patient record list,

1. Trackball to the patient’s name to highlight the name, (or perform a search to locate the patient) then press Select Patient.

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LOGI 3

Pre

Starti

New P

To star

1. Prthe

2. Se3. Ty

etc4. Pr

(Dau

5. Pr

Selection Window [2]nt is used to clear the patient entry screen to patient’s data into the database. Register is

ter new patient information into the database rforming the actual exam. Details displays ils and additional patient information.

p/Move [3] ethod to backup (move and delete patient

an external media.

4] s exam’s dataflow preference.

atient Menu and returns to scanning.

formation [6] Name, Birthdate, Age, and Sex.

Selection and Exam Information [7&8] appropriate category and enter the exam .

ew and Exam View [9]w lists the patients in the database. “Search les searching list by Patient ID, Last Name, , Birthdate, Sex and Last Exam date. “Search tring” fields help define the search parameters.

lists the exams of the selected patient. Select or the exam in Patient View and press “Exam eview“.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

paring for an Exam

ng an Exam

atient

t a new patient’s exam,

ess Patient. Press the New Patient button on Patient menu. lect the Exam Category. pe the Patient ID, Patient Name, Birthdate, .

ess the Register button on the Patient menu O NOT press Register if you are tomatically generating a patient ID). ess Scan, B-Mode, Esc, or Exit.

Probe Selection

Probes are selected from the Application Key. There are default applications associated with each probe. Therefore, after pressing New Patient, it is advisable to select the appropriate probe before entering patient data.

Patient Entry Menu

Image Management Window [1]

Access to this patient’s exam history and image management features.

Function New Patieinput a newused to enprior to peexam deta

EZ BackuOne-step mimages) to

Dataflow [Selects thi

Exit [5] Exits the P

Patient InPatient ID,

Category Select the information

Patient ViPatient VieKey” enabFirst Namekey” and “s

Exam Viewthe patientView” or “R

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LOGI 4

LOGI

Cont

1. TG2. Ne

the3. En4. Mo

(CPo(C

5. VoKe

6. ImBoCuke

7. Dead

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to 11. Fr12. Ke

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Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3

rol Panel Tour

C. Move slide pots left/right to adjust VCR.w Patient and Report: Press to activate se controls.d Exam: Press to end the exam.de/Gain Keys: M Mode, Continuous Wave

W) and Pulsed Wave Doppler (PW) Modes, wer Doppler Image Mode (PDI), Color Flow F) Mode, B Mode, and B Flow. lume, 3D, Harmonics and User Defined ys.aging/Measurement Keys: Clear, Comment, dy Pattern, Ellipse, Measure, Zoom, M/D, rsor, Scan Area, Set. Press or rotate these ys, as necessary.pth: Press the two-button function key to just the depth.verse: Press to invert the image left/right.aging Feature Keys: Auto Optimize On/Off, B use, Multi Image Left/Right Select. int Keys: Press the P1, P2, P3, and P4 keys archive, print or send the image.eeze: Press Freeze to freeze the image.yboard: Use the keyboard to enter the tient information and annotations.p and Sub Menu Controls: Activate the anges of functions in the Top/Sub Menus.ility Key: Press to select the presets.plications: Select the application to use and obe select.eral, the key status is indicated at the top of y.

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LOGI 5

Pre

LOGI

In genthey aPaddle

otate is used to turn on/off or change the eter selected through Top Menu

ols.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

paring for an Exam

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Top and Sub Menu Controls

eral, Top Menu Controls are of two types, re Push & Turn Knobs, Sub Menu is of Switch type

1. The Paddle Switch is used to select the Sub Menu controls.

2. The Push controls are used to select the Top Menu Controls.

3. The RparamContr

Top Menu Controls

1. Up2. Increase Value / Next Page3. Down4. Decrease Value / Previous Page

1 2 3 4 5

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LOGI 6

LOGI

1. InsIde

2. Pa3. Ac

tim4. GE

Cothe

5. Im6. Gr7. Ci

Scale.e Management Menu: Menu, Delete, and e Manager. Lock: On or Off.ce interface icon (wrench), iLinq icon, and m messages display.(not shown on the .ball Functionality Status: Scroll, (Measurement and Analysis), Position, Scan Area Width and Tilt.

enu

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Monitor Display Tour

titution/Hospital Name, Date, Time, Operator ntification.tient Name, Patient Identification.oustic Output Readout, System status (real-e or frozen) Symbol: Probe Orientation Marker. incides with a probe orientation marking on probe.age Preview.ay/Color Bar.ne Gauge.

8. Measurement Summary Window.9. Image.10. Measurement. 11. Results Window.12. Probe Identifier. Exam Study.13. Imaging Parameters by Mode (current mode

highlighted).14. Focus Marker.15. TGC (not shown on the image).16. Body Pattern.

17. Depth18. Imag

Imag19. Caps20. Servi

systeimage

21. TrackM&A Size,

22. Sub m

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LOGI 7

Pre

B/M M

Powe

Optimibeam Values

Dynam

Dynamconveradjusta

Focus

Increamovesthe becorreson the

NOTEand Fo

Rejec

Selectamplifiamplitu

Edge

Edge Eand bodifferestructuenhan

Control Panel Controls

timize

Tissue Optimization optimizes the image on a specified Region of Interest (ROI) or within the display.

a zoom region of interest, which is to approximately the size of a full-sized un-zoomed reference image is displayed

to the zoom window. The system adjusts g parameters accordingly. Press two-om key to activate. Press right Clr (Zoom y to deactivate. Use the Trackball to he Zoom ROI.

image left/right.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

paring for an Exam

ode Image Optimize

r Output

zes image quality and allows user to reduce intensity. 10% increments between 0-100%. greater than 0.1 are displayed.

ic Range

ic Range controls how echo intensities are ted to shades of gray, thereby increasing the ble range of contrast.

Number and Position

ses the number of transmit focal zones or the focal zone(s) so that you can tighten up am for a specific area. A graphic caret ponding to the focal zone position(s) appears right edge of the image.

: Push key to toggle between Focus Number cus Position.

tion

s a level below which echoes will not be ed (an echo must have a certain minimum de before it will be processed).

Enhance

nhance brings out subtle tissue differences undaries by enhancing the gray scale

nces corresponding to the edges of res. Adjustments to M Mode's edge cement affects the M Mode only.

Frame Average

Temporal filter that averages frames together. This has the effect of presenting a smoother, softer image.

Colorize

Enables gray scale image colorization. To deactivate, reselect a Gray Map.

Gray Map

Determines how the echo intensity levels received are presented as shades of gray.

Rotation (Up/Down)

Rotates the image by selecting the value from the pop up menu.

Frequency

Multi Frequency mode lets you downshift to the probe's next lowerfrequency or shift up to a higher frequency.Future Validation.

Frame Rate/Resolution

Optimizes B Mode frame rate or spatial resolution for the best possible image.

Anatomical M Mode

Allows you to move the M Mode trace in order to Image difficult -to - reach anatomy.

Sweep Speed

Changes the speed at which the time line is swept.

B Mode

Auto Op

Automaticbased upanatomy

Zoom

Magnifiesmagnifiedimage. Anadjacent all imaginbutton ZoClear) Keposition t

Reverse

Flips the

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LOGI 8

B/M M

B/M M

Auto Owhile r

Frequoptimiz

hance. Better delineates the amount of spness.

erage. Smooths the image by averaging ffects the amount of speckle reduction.

b Menu

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ode Image Optimize (continued)

ode Scanning Hints

ptimize. Improves imaging performance educing optimization time.

ency. Changes system parameters to best e for a particular patient type.

Maps. There is an inter-dependency between gray maps, gain, and dynamic range. If you change a map, revisit gain and dynamic range settings.

Dynamic Range. Affects the amount of gray scale information displayed. If you increase the gain, you may want to decrease the dynamic range.

Edge Enborder cri

Frame Avframes. A

B Mode Top Menu and Sub Menu M Mode Top Menu and Su

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LOGI 9

Pre

Color

Basel

Adjustslower

PRF/W

Velocitfrequeexceedautomgates

Wall Fexcess

NOTEFilter.

Angle

Estimato the betweemeasu

Auto

Adjust

Angle

SlantsDopple

Thres

Threshcolor in

s in Common with B Mode

information on Focal Zone, Power Output, Frame Averaging, Dynamic Range, Map, ize, refer to the B/M Mode Image section in this Quick Guide on Page 6.

g Hints

sity. Trades frame rate for sensitivity and solution. If the frame rate is too slow, e size of the region of interest, select a ine density setting, or reduce the packet

r. Affects low flow sensitivity versus tifact.

e sensitivity.

ase the Gain. ase the PRF.

ase the Power Output. t the Line Density. ase the Wall Filter.

ase Frame Averaging. ase the Packet Size. ce the ROI to the smallest reasonable

ion the Focal Zones properly.

se motion artifact,

ase the PRF. ase the Wall Filter.

te aliasing,

ase the PRF. r the Baseline.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

paring for an Exam

Flow/Doppler Image Optimize

ine

s the baseline to accommodate faster or blood flows to eliminate aliasing.

all Filter

y scale determines pulse repetition ncy. If the sample volume gate range s single gate PRF capability, the system

atically switches to high PRF mode. Multiple appear, and HPRF is indicated on the display.

ilter insulates the Doppler signal from ive noise caused from vessel movement.

: Push key to toggle between PRF and Wall

Correct

tes the flow velocity in a direction at an angle Doppler vector by computing the angle n the Doppler vector and the flow to be red.

Angle

e the angle to the direction of the Flow.

Steer

the Color Flow region of interest or the M Line to obtain a better doppler angle.

hold

old assigns the gray scale level at which formation stops.

Doppler Display Formats

Display layout can be preset to have B-Mode and Time-motion side-by-side or over-under.

Sample Volume Gate Length

Sizes the sample volume gate.

Map

Allows a specific color map to be selected. After a selection has been made, the color bar displays the resultant map.

Packet Size

Controls the number of samples gathered for a single color flow vector.

Invert

Allows blood flow to be viewed from a different perspective, i.e. red away (negative velocities) and blue toward (positive velocities). The real-time or frozen image can be inverted.

Color Flow Control Panel Control

Scan Area

Toggles between the CFM window size and position.

Control

For moreFR/RES, and ColorOptimize

Scannin

Line Denspatial rereduce thdifferent lsize.

Wall Filtemotion ar

To improv

1. Incre2. Decre3. Incre4. Adjus5. Decre6. Incre7. Incre8. Redu

size. 9. Posit

To decrea

1. Incre2. Incre

To elimina

1. Incre2. Lowe

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LOGI 10

Color

For ven

1. Ensexa

2. Sel

te Color Flow. in the PRF at a lower setting. se Frame Averaging for more tence.

p and Sub Menu

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Flow/Doppler Image Optimize (continued)

ous imaging,

ure that you have selected the small parts m category. ect a venous application.

3. Select the appropriate probe for very superficial structure.

4. Select two focal zones. 5. Adjust the depth to the anatomy to be imaged. 6. Maintain a low gain setting for gray scale.

7. Activa8. Mainta9. Increa

persis

CFM Mode Top and Sub Menu PWD Mode To

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LOGI 11

Pre

Basic

NOTEfirst sc

Distan

1. Prdis

2. To(dide

3. Tofixac

4. Topo(tis

5. Tosyva

NOTE

NOTEerase but no

erence/Area (Trace) Measurement

Measure twice; a trace caliper displays.sition the trace caliper at the start point, the Trackball. the trace start point, press Set. The trace r changes to an active caliper.ce the measurement area, move the ball around the anatomy. A dotted line

s the traced area.o erase the dotted line but not the trace ess Clear once. To clear the trace caliper urrent data measured, press Clear twice.

o erase the line (bit by bit) back from its int, move the Trackball or turn the

ontrol counterclockwise.

mplete the measurement, press Set. The m displays the circumference and the area measurement results window.efore you complete a measurement:

o erase the line (bit by bit) back from its urrent point, move the Trackball or turn the llipse control counterclockwise.o erase the dotted line but not the trace aliper, press Clear once.o clear the trace caliper and the current ata measured, press Clear twice.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

paring for an Exam

Measurements

: The following instructions assume that you an the patient and then press Freeze.

ce and Tissue Depth Measurements

ess Measure once; an active caliper plays. position the active caliper at the start point stance) or the most anterior point (tissue pth), move the Trackball. fix the start point, press Set. The system es the first caliper and displays a second tive caliper. position the second active caliper at the end int (distance) or the most posterior point sue depth), move the Trackball.

complete the measurement, press Set. The stem displays the distance or tissue depth lue in the measurement results window.: Before you complete a measurement:

To toggle between active calipers, press Measure.To erase the second caliper and the current data measured and start the measurement again, press Clear once.

: After you complete the measurement, to all data that has been measured to this point, t data entered onto worksheets, press Clear.

Circumference/Area (Ellipse) Measurement

1. Press Measure once; an active caliper displays.

2. To position the active caliper, move the Trackball.

3. To fix the start point, press Set. The system fixes the first caliper and displays a second active caliper.

4. To position the second caliper, move the Trackball.

5. Turn the Ellipse control; an ellipse with an initial circle shape appears.

NOTE: Be careful not to press the Ellipse control as this activates the Body Pattern.

6. To position the ellipse and to size the measured axes (move the calipers), move the Trackball.

7. To increase the size, Turn the Ellipse control in a clockwise direction. To decrease the size, turn the Ellipse control in a counterclockwise direction.

8. To toggle between active calipers, press Measure.

9. To complete the measurement, press Set. The system displays the circumference and area in the measurement results window.

NOTE: Before you complete a measurement:

To erase the ellipse and the current data measured, press Clear once. The original caliper is displayed to restart the measurement.To exit the measurement function without completing the measurement, press Clear a second time.

Circumf

1. Press2. To po

move3. To fix

calipe4. To tra

Trackshow

NOTE: Tcaliper, prand the c

NOTE: Tcurrent poEllipse c

5. To cosystein the

NOTE: B

TcETcTd

Page 16: L3_QG_5122541_4_100

LOGI 12

Volum

1. Tofol

• Ma• Ma• Ma

NOdumepla

• Mame

• Ma2. Se

Time

1. Prve

2. Tomo

3. Tofixac

4. Tomo

5. Tosytwwi

eets

ent/Calculation worksheets are available and edit measurements and calculations. generic worksheets as well as n specific worksheets. The worksheets

ted from the Measurement Top/Sub Menu.

Pages

ents/Calculations that are included on heet can also be displayed on Report eport Pages can be customized to meet priate needs of the user.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

e

make a volume calculation, do one of the lowing:ke one distance measurement.ke two distance measurements.ke three distance measurements.TE: Three distances should be done in the

al format mode (side by side images). One asurement is usually made in the sagittal ne and two measurements in the axial plane.

ke one distance and one ellipse asurement.ke one ellipse measurement.lect Volume.

Interval Measurement

ess Measure twice; and active caliper with a rtical dotted line displays. position the active caliper at the start point, ve the Trackball.

fix the start point, press Set. The system es the first caliper and displays a second tive caliper. position the second caliper at the end point, ve the Trackball.

complete the measurement, press Set. The stem displays the time interval between the o calipers in the measurement results ndow.

Velocity Measurement

1. Press Measure; an active caliper with a vertical dotted line displays.

2. To position the caliper at the desired measurement point, move the Trackball.

3. To complete the measurement, press Set. The system displays the velocity measurement in the measurement results window.

PI, RI, S/D Ratio, D/S Ratio or A/B Ratio

Select PI, RI, S/D Ratio, A/B Ratio or D/S Ratio from the Doppler Primary & Secondary Controls. Perform velocity measurements.

1. The first caliper is the start point on the Doppler waveform. This would be VMAX for PI, peak velocity for RI, systole for S/D ratio, “A” velocity for A/B ratio or diastole for D/S ratio.

2. The second caliper is the end-point caliper to the end point of the Doppler waveform. This would be Vd for PI, minimum velocity for RI, diastole for S/D ratio, “B” velocity for A/B ratio or systole for D/S ratio.

NOTE: For the PI calculation, if Trace Auto is not selected, manually trace the waveform between VMAX and Vd.

NOTE: For the PI calculation, if Trace Auto is on, the system automatically traces the waveform when Set is pressed to fix Vd.

Worksh

Measuremto displayThere areApplicatioare selec

Report

Measuremthe worksPages. Rthe appro

Page 17: L3_QG_5122541_4_100

LOGI 13

Using

Conn

1. Plasu

2. Capro

3. DOImirre

4. Tu

5. Alica

6. Tuse

7. Cacores

Activa

Selectindicat

The properatmode

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Using Probes

Probes

ecting a probe

ce the probe's carrying case on a stable rface and open the case.refully remove the probe and unwrap the be cable. NOT allow the probe head to hang free.

pact to the probe head could result in parable damage.

rn the connector locking handle clockwise.

gn the connector with the probe port and refully push into place.rn the connector locking handle clockwise to cure the probe connector.refully position the probe cable in the probe rd holder spot so it is free to move, but not ting on the floor.

ting the probe

the appropriate probe from the probe ors on the Top/Sub Menu.

obe activates in the currently-selected ing mode. The probe's default settings for the and selected exam are used automatically.

Deactivating the probe

When deactivating the probe, the probe is automatically placed in standby mode.

1. Press the Freeze key.2. Gently wipe the excess gel from the face of the

probe. 3. Carefully slide the probe around the right side

of the keyboard, toward the probe holder. Ensure that the probe is placed gently in the probe holder.

Disconnecting the probe

Probes can be disconnected at any time. However, the probe should not be selected as the active probe.

1. Move the probe locking handle counterclockwise. Pull the probe and connector straight out of the probe port.

2. Carefully slide the probe and connector away from the probe port and around the right side of the keyboard. Ensure the cable is free.

3. Be sure that the probe head is clean before placing the probe in its storage box.

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LOGI 14

Prob

Prob

12L

X

X

X

X

X

X

X

L 12L BE9C

X X

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

es Application

es Features

Table 1-1: Probe Indications for Use

Probe Application 3C 3.5C 5C E8C 10LB 3S 7S 8C 10L 8L BE9C

Abdomen X X X X X X X X

Small Parts X X X X X X

Periph. Vasc. X X X X

Obstetrics X X X X X X X X

Gynecology X X X X X X X X

Pediatrics X X X X X X

Neonatal X X X X

Urology X X X X X X

Surgery

Cardiac X X

Endocavity

Transcranial X

Table 1-2: Probe Features

Probe Feature 3C 3.5C 5C E8C 10LB 3S 7S 8C 8L 10

Virtual Convex X

Easy 3D (Option) X X X X X X X

Advanced 3D (Option) X X X X X X X

Anatomical M X X X X X X X

Steerable CWD X X

Biopsy X X X X X X X X

Page 19: L3_QG_5122541_4_100

LOGI 15

Prob

Probe

hen handling and protect from damage when not in ipment damage.

llow these precautions can result in serious injury

ector or probe adapters into any liquid.

drogen peroxide

amaged or defective probe.

t user to verify and maintain the effectiveness of the e procedures.

robes for neuro surgical use must not be sterilized

oroughly clean the probe, as described on the

isinfecting means.

e solution:e probe connector or probe adaptors into any liquid.ge such as cracks or chips in the housing may

rough inspection should be conducted during the

the service manual for leakage check procedures.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Using Probes

e Cleaning and Disinfection Instructions

Safety

WARNING Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use care wuse. DO NOT use a damaged or defective probe. Failure to follow these precautions can result in serious injury and equ

Ultrasound transducers can easily be damaged by improper handling and by contact with certain chemicals. Failure to foand equipment damage.• Do not immerse the probe into any liquid beyond the level specified for that probe. Never immerse the transducer conn• Avoid mechanical shock or impact to the transducer and do not apply excessive bending or pulling force to the cable.• Transducer damage can result from contact with inappropriate coupling or cleaning agents:

• Do not soak or saturate transducers with solutions containing alcohol, bleach, ammonium chloride compounds or hy• Avoid contact with solutions or coupling gels containing mineral oil or lanolin• Avoid temperatures above 60°C.• Inspect the probe prior to use for damage or degeneration to the housing, strain relief, lens and seal. Do not use a d

BiologicalHazard

CAUTION Adequate cleaning and disinfection are necessary to prevent disease transmission. It is the responsibility of the equipmeninfection control procedures in use. Always use sterile, legally marketed probe sheaths for intra-cavitary and intra-operativ

For neurological intra-operative procedures, use of a legally marketed, sterile, pyrogen free probe sheath is REQUIRED. Pwith liquid chemical sterilants because of the possibility of neuro toxic residues remaining on the probe.

A defective probe or excessive force can cause patient injury or probe damage:• Observe depth markings and do not apply excessive force when inserting or manipulating intercavity probes.• Inspect probes for sharp edges or rough surfaces that could injure sensitive tissue.

In order for liquid chemical germicides to be effective, all visible residue must be removed during the cleaning process. Thfollowing page before attempting disinfection.

CREUTZFIELD-JACOB DISEASE Neurological use on patients with this disease must be avoided. If a probe becomes contaminated, there is no adequate d

Electrical Hazard

The probe is driven with electrical energy that can injure the patient or user if live internal parts are contacted by conductiv• DO NOT immerse the probe into any liquid beyond the level indicated by the immersion level diagram. Never immerse th• DO NOT drop the probes or subject them to other types of mechanical shock or impact. Degraded performance or dama

result.• Inspect the probe before and after each use for damage or degradation to the housing, strain relief, lens, and seal. A tho

cleaning process.• DO NOT kink, tightly coil, or apply excessive force on the probe cable. Insulation failure may result.• Electrical leakage checks should be performed on a routine basis by GE Service or qualified hospital personnel. Refer to

Page 20: L3_QG_5122541_4_100

LOGI 16

Probe

1. Diremwi

2. Wwaspresso(suma

3. Riwa

4. Air

Probe

1. Prmapre

2. Plawigeis reqprorecPrmustetoxNeuspro

3. Afprorinres

isinfection Agents

d probes can be disinfected using liquid germicides. The level of disinfection is lated to the duration of contact with the . Increased contact time produces a el of disinfection.

ing high level disinfectant agents have roved for use with all probes:

x OPAxs has been approved for the 8C, 4DE7C, -L probes.

high level disinfectant has been approved , 10L, 12L, 4S, 8C, E8C, and P8D probes.

high level disinfectant has been for the 7L, 10L, 12L, M7C, M12L, E8C, D3C-L, and 4D10L probes.

ing low level disinfect agents have been for use with all probes:

Blu

th HB (Wipes)

nd T-Spray II low level disinfectant has roved for the 7L, 10L, 12L, M7C, M12L, 4DE7C, 4D3C-L, and 4D10L probes.

6 low level disinfectant has been for the 7L, 10L, 12L, M7C, M12L, and es.

test disinfectant recommendations, refer be Care Card or go to the GE Medical

Ultrasound web site:

emedicalsystems.com/rad/us/probe_care

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Cleaning, After Each Use

sconnect probe from ultrasound console and ove all coupling gel from probe by wiping

th a soft cloth and rinsing with flowing water. ash the probe with mild soap in lukewarm ter. Scrub the probe as needed using a soft onge, gauze, or cloth to remove all visible idue from the probe surface. Prolonged

aking or scrubbing with a soft bristle brush ch as a toothbrush) may be necessary if terial has dried onto the probe surface.

nse the probe with enough clean potable ter to remove all visible soap residue. dry or dry with a soft cloth.

Disinfection, After Each Use

epare the germicide solution according to the nufacturer's instructions. Be sure to follow all cautions for storage, use and disposal.ce the cleaned and dried probe in contact

th the germicide for the time specified by the rmicide manufacturer. High-level disinfection recommended for surface probes and is uired for endocavitary and intraoperative bes (follow the germicide manufacturer's ommended time).

obes for neuro surgical intra-operative use st NOT be sterilized with liquid chemical rilants because of the possibility of neuro ic residues remaining on the probe. urological procedures must be done with the e of legally marketed, sterile, pyrogen free be sheaths.

ter removing from the germicide, rinse the be following the germicide manufacturer's

sing instructions. Flush all visible germicide idue from the probe and allow to air dry.

Probe Immersion Levels

1. Fluid Level2. Aperture3. Contact face within patient environment

Probe D

Ultrasounchemical directly regermicidehigher lev

The followbeen app

• Cide• Cide

Cidex Pluand 4D3C

Sporox II for the 7L

Pera Safeapproved4DE7C, 4

The followapproved

• Ster Bac

• Sani-Clo

T-Spray abeen app4S, E8C,

Virex II 25approvedE8C prob

For the lato the ProSystems

Radiology

http://www.g

Page 21: L3_QG_5122541_4_100

LOGI 17

Imag

Clipb

As imakeys (PbottomthumbTheseof the

Printi

Press For mobutton

Brow

‘MouseSet to

Mana

From tNew P

Deleti

Selectonscre

Or, goof the be delfrom th

Up Patient Information

CD/MOD prior to following these steps.

t the Utility key. Select System, then up/Restore. t the media.

t the parameter under Backup by placing ck mark. Then press Backup. er ‘OK’ to the Back-Up pop-up message.he detailed section of this menu s the user defined configuration above. s you to selectively restore what you want across multiple machines.

O NOT restore service back-ups across rom one LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ to another LOGIQ 3 Expert/LOGIQ 3 Pro/system).

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Image Management

e Management

oard

ges are saved by pressing any of the print 1, P2, P3, or P4), the images appear at the

of the display on the clipboard as nails of the images saved during the exam. images remain on the clipboard until the end exam.

ng Images

the appropriate print key (P1, P2, P3, or P4). re information on programming the Print

s, See “Dataflow” on page 20.

sing an Exam’s Stored Images

over’ the image in the clipboard, then press view an enlarged thumbnail image.

ging an Exam’s Stored Images

he Display, press Active Images; from the atient menu, open Active Images.

ng an Image

the image on the clipboard, then press the en Delete shortcut.

to Active Images (lower, right-hand portion display). Highlight all the images that need to eted and press Delete All Temp Images e Top/Sub Menu

Formatting a CD/DVD/MOD

1. Insert the backup media. Format the backup media, CD or MOD. Select the Utility key. Select Connect, then Removable media. Label the media appropriately. Press Format.

2. The Ultrasound system displays a pop-up menu when the formatting has been completed. Press Ok to continue. Verify that the format was successful.

Backing

Format a

1. SelecBack

2. Selec

3. Seleca che

4. AnswNOTE: TdecoupleThis allowto restore

NOTE: Dsystems (f3 system LOGIQ 3

CAUTION DO NOT use CD-RW.

Page 22: L3_QG_5122541_4_100

LOGI 18

Movi

There and M

Impor

1. Atrem

2. Pr3. Se4. Se

do5. Se

To6. Se

Tr7. Pr8. W

pre

Expor

1. Fo2. Pr3. Se4. Se

Fr5. Se

Tr6. Se

do7. Pr

du8. Pr

wa

t the CD-R from the Transfer To pull-down .t the patient(s) or exam(s) from the list.: If you press the Clear button in the

fer From and Transfer To section, all the h criteria is cleared and the list is hed accordingly.

Transfer. The progress bar displays g the transfer.

the DICOM device

Patienth and select the patient and press Exam. atient Exam screen displays.t the exam which has the images and Send To.: You can only select the Local Archive-

D for Workflow.

end To dialogue box displays. Choose the ation device and select OK.: The destination device is configured in

tility screen. Multiple devices are able to nfigured.

uccessful/unsuccessful message is yed at the bottom of the screen.

you press the Clear button in the Transfer Transfer To section, all the search criteria is d the list is refreshed accordingly.

LWAYS exit to scanning after any Data function to ensure that the operation pleted.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ng Data Between Ultrasound Systems

are 5 options (Import, Export, Q/R, Worklist PEGvue) under Exam Data Transfer.

t

the other Ultrasound system, insert the ovable media.

ess Patient and select Exam Data Transfer.lect Import. lect the media from the Transfer From pull-wn menu. lect Local Archive-Int. HD from the Transfer pull-down menu. lect the patient(s) or exam(s) from the

ansfer From Search field for import. ess Transfer. ait until the patient information is copied and ss F3 when finished to eject the media.

t

rmat and label the removable media. ess Patient and select Exam Data Transfer.lect Export. lect Local Archive-Int. HD from the Transfer

om pull-down menu. lect the patient(s) or exam(s) to export in the

ansfer From Search field (the top portion). lect the destination at the Transfer To pull-wn menu.ess Transfer. The progress bar displays ring the transfer.ess F3 to eject the media. Specify that you nt to finalize the CD or DVD.

Query/Retrieve (Q/R)

1. Press Patient and select Exam Data Transfer.2. Select Q/R. The local archive is enabled for the

transfer process.3. Select the Query/Retrieve server from the

Transfer From pull-down menu.4. Press Query in the Transfer From section. The

server’s patient list displays.5. Select the patient(s) or exam(s) to retrieve from

the patient list.6. Press Transfer. The data is retrieved from the

server as the progress bar displays.

Worklist

1. Press Patient and select Exam Data Transfer.2. Select Worklist. The last Worklist used

displays on the monitor. 3. Press Refresh to refresh the list or select

another Worklist server from the transfer From pull-down menu.

4. Select the patient(s) or exam(s) from the list.5. Press Transfer. The progress bar displays

during the transfer.

MPEGvue

Save the data to CD-R to view on PC

1. Format and label the CD-R. 2. Press Patient and select Exam Data Transfer.3. Select MPEGvue. The patient list in the Local

Archive-Int. HD displays in the Transfer From section.

4. Selecmenu

5. SelecNOTETranssearcrefres

6. Pressdurin

Send To

1. Press2. Searc

The P3. Selec

pressNOTEInt. H

4. The SdestinNOTEthe Ube co

5. The sdispla

NOTE: IfFrom and cleared an

NOTE: ATransfer has com

Page 23: L3_QG_5122541_4_100

LOGI 19

EZBa

NOTEhard dwhile mscanneand im

1. TotheMoThNOmisasc

2. VeEZNObeonpa

3. VeWmehabe

4. A wiins

e Computer’s Name (better known as the Identify the Ultrasound system to the rest work by filling in its IP Address, Subnet d Gateway (if applicable). Press Save.

Figure 1-1.

D

Add. the name of the device and its IP address. Save.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Image Management

ckup/Move

: EZBackup/Move allows you to manage isk space (move images off the hard drive)

aintaining the patient database on the r, as well as to back up the patient database ages.

start the EZBackup/Move procedure, go to Patient menu and select the EZBackup/ve button at the bottom of the Patient list. e EZBackup/Move Wizard starts.TE: EZBackup/Move can take up to 20

nutes. Make sure to schedule this at the me time daily, when no patients are heduled.

rify the information on the first page of the Backup/Move Wizard, then press Next. TE: If the EZBackup/Move presets need to

modified, those requirements are specified the Utility --> System --> Backup/Restore ge.

rify the information on the EZBackup/Move izard, Page 2. This page tells you how many dias you need to do this backup. After you ve gathered the media, you are ready to gin the backup. Press Next. pop-up message appears that provides you th the media label. Label the media, then ert the media. Press OK.

5. The status menu appears.NOTE: When/if you need to insert the next media, a message appears providing you with the media label a well. Label the media, then insert the media and press OK.

6. When the backup is complete, the Backup completed page appears.

NOTE: To view the media, do so via the Patient menu by selecting the patient and loading the appropriate media, or via Import, or via DICOM CD View.

Connectivity

Connectivity on the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 is based on the Dataflow concept.

Login as Administrator. Select Utility. Select Connect. Configure the menus from left to right, starting with TCP/IP first. When finished making connectivity changes to the utility menus, restart the system.

TCP/IP

Type in thAE Title).of the netMask, an

Device

1. Press2. Type 3. Press

Page 24: L3_QG_5122541_4_100

LOGI 20

Servic

To add

1. Se2. Se3. Ty4. Sp

in sid

5. Pr

There

• Sta• Vid

arean

ssign print buttons to a device or to a

t the print button to configure and the rties on the left of the screen.t the service you want to use under My uter and press >> to add to Printflow

: Select the Standard Print under Active es Page as necessary.

Save.

: You can configure each print key to le output devices/workflow.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

es

the services,

lect the destination device.lect the service to add and press Add.pe the name in the Name Field.ecify criteria in the Properties boxes (located the upper right-hand side and lower left-hand e).

ess Save.

are two service types that pertain to printers:

ndard Printer is used for digital peripherals. eo Capture Device is used for devices that triggered by a contact closure, typically

alog devices.

Dataflow

The Dataflow page allows you to add services to the selected dataflow. For example, DICOM services may be for storage, worklist, verify, etc. In addition, there are other service types like video print or standard color print

Set up dataflows for the services.

1. Press Add and type the dataflow name in the name field.

2. Select the service you want to use under My Computer and press >> to add to Dataflow view.

3. Press Verify, then Save.

NOTE: Query/Retrieve MUST be the only service in a dataflow.

NOTE: Set Query/Retrieve to Hidden so that it cannot be selected from the Patient Menu.

Buttons

You can adataflow.

1. Selecprope

2. SelecCompview.NOTEImag

3. Press

NOTEmultip

Page 25: L3_QG_5122541_4_100

LOGI 21

Remo

Forma

Misce

Set upStore O

tatus

the status of all DICOM jobs or redirect bs, press F4.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Image Management

vable Media

t and verifying media.

llaneous

Patient/Exam menu options and Printer and ptions

Saving Images as JPEG files and CINE Loops as AVI files

Format a CD/MOD prior to following these steps.

1. Press Menu (on the lower, right-hand portion of the display) and select Save As. The SAVE AS menu appears.

2. Specify Compression and Save As Type and press Save. The image is saved to the CD/MOD.

3. When you have saved all the images you want on the CD/DVD//MOD, remove the media (press F3 to eject the CD/DVD).

4. Finalize the CD by selecting Yes. The media is ejected from the system.

NOTE: If you want to add more images to the media , select “No” and do not finalize the media.

DICOM S

To check DICOM jo

Page 26: L3_QG_5122541_4_100

LOGI 22

Using

Activa

Press CINE. Stop. T

Quick

Press Last to

through a CINE Loop Frame By

e by Frame to move throuh CINE ne frame at a time.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

CINE

ting CINE

Freeze, then roll the Trackball to activate To start CINE Loop playback, press Run/o stop CINE Loop playback. press Run/Stop.

ly Move to Start/End Frame

First to move to the first CINE frame; press move to the last CINE frame.

Start Frame/End Frame

Turn the Start Frame dial to the left to move to the beginning of the CINE Loop. Turn the dial to the right to move forward through the CINE Loop.

Turn the End Frame dial to the right to move to the end of the CINE Loop. Turn the dial to the left to move backward through the CINE Loop.

Adjusting the CINE Loop Playback Speed

Turn the Loop Speed dial right/left to increase/decrease the CINE Loop playback speed.

Moving Frame

Turn Frammemory o

Page 27: L3_QG_5122541_4_100

LOGI 23

Easy

Acqu

1. Opco

2. Prap

3. Tosp

4. Topeon

5. Thas

NOTEscanniagain.

6. Tosp

NOTEneed trender

ing a Surface Render

3D Top Menu press Texture to add a istic/clay-like quality to the render.

opacity and density via Threshold/press the key to adjust opacity). This hat ‘grays’ the system recognizes, ou to emphasize/de-emphasize grays as

y.

l away portions of the anatomy,

Scalpel. A caliper appears on the 3D

Set to set the caliper. Trackball around ortion to be cut away. le click and apply the scalpel. ge the projection and scalpel again.

ou can undo one scalpel.

Scanning Hints

ppropriate values for the 3D Acq Mode Plane.

able to set the scan distance before the ins.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

Using Cine

3D (option)

iring a 3D Scan

timize the B-Mode image. Ensure even gel verage. ess the 3D control panel key. Two screens pear. start acquiring the image, press ‘L’ (the left lit screen key). perform a parallel scan, scan evenly. To rform a sweep (fan) scan, rock the probe ce. Note the distance of the scan. e 3D volume of interest is dynamically sembled on the right side of the screen.

: If the image stops before you’re done ng, start acquiring the 3D volume of interest

complete the 3D scan, press ‘R’ (the right lit screen key).

: You can also press Freeze, but then you o also press the 3D key to obtain the final .

Manipulating the 3D Scan

Imagine you are able to manipulate the 3D volume of interest (VOI) in your hand.

You can rotate it left to right or right to left. You can rotate it forward/backward (white hand).

Then, imagine that you can view the volume of interest one slice at a time through the anatomy (red hand).

Also imagine that you are able to pull back tissue to view specific portions of anatomy (yellow and green hands).

The 3D volume of interest is a tangible anatomical object that you can see and manipulate easily using the Trackball and Set control panel keys.

Practice positioning the pointer at different places within the 3D volume of interest. Highlight different colors, press Set to select this volume for manipulation. Use the hand to move the 3D volume.

Adjusting the 3D Volume of Interest

You can colorize the 3D volume of interest.

You can resize the VOI by adjusting the scan distance.

Perform

From the photoreal

Adjust theOpacity (adjusts wallowing ynecessar

Scalpel

To scalpe

1. PressVOI.

2. Pressthe p

3. Doub4. Chan

NOTE: Y

3DView

Set the aand Scan

It is advisscan beg

Page 28: L3_QG_5122541_4_100

LOGI 24

Conta

INTER

http://w

USA

GE MeUltraso4855 WMilwauTEL: (

Clinic

For infMexicoCustomTEL: (In otheSales

Servic

For seTEL: (

Acces

To reqequipmRespoIn otheSales

ound Asia TEL: 65-291-8528 On-Line LC), Asia FAX: 65-272-3997

awa medical system (inc.) call center TEL: 0120-055-919

INA

A.237ires - 140739-1619 -- FAX: (1) 567-2678

bH Medical Systems Austria en Strasse 8/8 IEN

3140 8459 toll free -- FAX: +43 1 505 38 74

al Systems Beneluxdestraat 3 OMMELGEM 0 11733 toll free 0 3 320 12 5922

as Médicosde Julho 52297 São Paulo SP0-122345 -- FAX: (011) 3067-8298

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev.4

ct Information

NET

ww.gemedicalsystems.com

dical Systemsund Service Engineering. Electric Avenue

kee, WI 532191) 800-437-1171 or FAX: (1) 414-647-4090

al Questions

ormation in the United States, Canada, and parts of the Caribbean, call the er Answer Center:

1) 800-682-5327 or (1) 262-524-5698r locations, contact your local Applications, or Service Representative.

e Questions

rvice in the United States, call GE CARES 1) 800-437-1171

sories Catalog Requests

uest the latest GE Accessories catalog or ent brochures in the United States, call the

nse Center: TEL: (1) 800-643-6439r locations, contact your local Applications, or Service Representative.

Placing an Order

To place an order, order supplies or ask an accesory-related question in the United States, call the GE Access Center: TEL: (1) 800-472-3666In other locations, contact your local Applications, Sales or Service Representative.

OTHER COUNTRIES

NO TOLL FREE TEL: international code + 33 1 39 20 0007

CANADA

GE Medical SystemsUltrasound Svc Engineering TEL: (1) 800-664-07324855 W. Electric AvenueMilwaukee, WI 53219Customer Answer Center TEL: (1) 262-524-5698

LATIN & SOUTH AMERICA

GE Medical SystemsUltrasound Svc Engineering TEL: (1) 305-735-23044855 W. Electric AvenueMilwaukee, WI 53219Customer Answer Center TEL: (1) 262-524-5698

EUROPE

GE Ultraschall Deutschland GmbH & Co. KGBeethovenstraße 239Postfach 11 05 60D-42655 Solingen -- TEL: 0130 81 6370 toll freeTEL: (49) 212.28.02.207 -- FAX: (49) 212.28.02.431

ASIA

GE UltrasCenter (O

JAPANGE Yokogcustomer

ARGENT

GEME S.Miranda 5Buenos ATEL: (1) 6

AUSTRIA

GE GesmPrinz EugA-1040 WTLX: 136TEL: 066

BELGIUM

GE MedicGulkenroB-2160 WTEL: 0 80FAX: +32TLX: 727

BRAZIL

GE SistemAv Nove 01407-90TEL: 080

Page 29: L3_QG_5122541_4_100

LOGI 25

tion

DENM

GE MeFabrikDK-26TEL: +

FRAN

GE Me738 ruF-9265TEL: 0

GERM

GE UltDeutscBeethoPostfaD-426TEL: 0TEL: (4

GREE

GE Me41, NikG-171TEL: +

ITALY

GE MeVia MoI-2005TEL: 1TLX: 3

al Systems España rturo Gimeno

Industrial ITORREJON DE ARDOZ95 3349 free -- FAX: +34 1 675 336484 A/B GEMDE

N

al Systems1243KISTA 795 433 toll free -- FAX: +46 87 51 30 9028 CGRSWES

LAND

al Systems (Schweiz) AG tweg 1 KRIENS 5306 -- FAX: +41 41 421859

Sys. Turkiye A.S. ehliran Sodakn, No 24 Kat 1peL 212 75 5552 -- FAX: +90 212 211 2571

KINGDOM

al SystemsHouseingham Avenue

SL1 4ER0 89 7905 toll free -- FAX: +44 753 696067

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev.4

Contact Informa

ARK

dical Systems sparken 20 00 GLOSTRUP45 4348 5400 -- FAX: +45 4348 5399

CE

dical Systems e Yves Carmen 8 BOULOGNE CEDEX5 49 33 71 toll free -- FAX: +33 1 46 10 01 20

ANY

raschallhland GmbH & Co. KGvenstraße 239

ch 11 05 6055 Solingen130 81 6370 toll free9) 212.28.02.207 -- FAX: (49) 212.28.02.431

CE

dical Systems Hellasolaou Plastira Street

21 NEA SMYRNI30 1 93 24 582 -- FAX: +30 1 93 58 414

dical Systems Italiante Albenza 92 MONZA 678 744 73 toll free -- FAX: +39 39 73 37 86333 28

LUXEMBOURG

TEL: 0800 2603 toll free

MEXICO

GE Sistemas Médicos de Mexico S.A. de C.V.Rio Lerma #302, 1º y 2º PisosColonia Cuauhtémoc06500-México, D.F.TEL: (5) 228-9600 -- FAX: (5) 211-4631

NETHERLANDS

GE Medical Systems Nederland B.V. Atoomweg 512 NL-3542 AB UTRECHTTEL: 06 022 3797 toll free -- FAX: +31 304 11702

POLAND

GE Medical Systems PolskaKrzywickiego 34P-02-078 WARSZAWATEL: +48 2 625 59 62 -- FAX: +48 2 615 59 66

PORTUGAL

GE Medical Systems Portuguesa S.A.Rua Sa da Bandeira, 585Apartado 4094 TLX: 22804P-4002 PORTO CODEXTEL: 05 05 33 7313 toll free - FAX: +351 2 2084494

RUSSIA

GE VNIIEMMantulinskaya UI. 5A123100 MOSCOW TEL: +7 095 956 7037 -- FAX: +7 502 220 32 59TLX: 613020 GEMED SU

SPAIN

GE MedicHierro 1 APoligono E-28850 TEL:900 TLX: 223

SWEDE

GE MedicPO-BOX S-16428 TEL: 020TLX: 122

SWITZER

GE MedicSternmatCH-6010TEL: 155

TURKEY

GE Med. Mevluk PYilmaz HaGayrettepISTANBUTEL: +90

UNITED

GE MedicCoolidge 352 BuckSLOUGHBerkshireTEL: 080

Page 30: L3_QG_5122541_4_100

LOGI 26

Docu

Introd

Docum

• On• Ba• Ad• Qu• Qu• Re• Ba

ng Through Help

lp is organized like a manual, with chapters, sections, and pages.

he plus (+) sign next to MANUAL to open ok.

he plus sign next to the chapter you want open up that chapter.

he plus sign next to the chapter you want open up that section.

pen up the page to view that page’s n.

underlined text links you to related topics. he link to move to the new topic.

k to the previous screen, press Back. To he link, press Forward.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

mentation

uction

entation is being provided via:

line Help (on the Ultrasound Scanner via F1)sic User Manualvanced Reference Manualick Guideick Card(s)lease Notes and Workaroundssic Service Manual

Using Online Help Via F1 (Only English)

Online Help is available via the F1 key.

The Help screen is divided into three sections:

• navigational tools on the top, left portion of the screen (Hide, Back, Forward)

• help book navigational tools on the left portion of the screen (Contents, Index, Search, Favorites)

• content portion on the right side of the screen where help topics are displayed

Navigati

Online Heindividual

Click on tup the bo

Click on tto view to

Click on tto view to

Click to oinformatio

The blue,Click on t

To go bacreturn to t

Page 31: L3_QG_5122541_4_100

LOGI 27

tation

Help L

After ythe scr

Searc

To seatab. Tykeywophrasedisplaywant toDispla

e Help Index

n look for topics by using the Index. Press tab, then use the scroll bar to look up a

elp Features

e left side of the screen, press the Hide upper, left-hand portion of the screen. To

eft side of the screen again, press the n at the upper, left-hand portion of the

e Help window, position and hold down r at the corner of the screen while moving ball.

the Help window to the Touch Panel osition and hold down the cursor at the f the Help window while moving the

to the Touch Panel display.

nline Help

line Help, press the ‘X’ in the upper, right-er of the Online Help window.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick GuideDirection 5122541-100 Rev. 4

Electronic Documen

inks

ou click on a blue, underlined portion of text, een updates with this link’s content.

hing for a Topic in Help

rch for a specific topic, click on the Search pe in the topic name in the Type in the rd to find: field. Topics with the word or you typed appear in the Select Topic to : area. Either double click on the topic you view or highlight the topic and press the

y button to view this topic.

Creating a List of Favorite Topics in Help

You may find that there are topics you need to refer to often. In this case, it’s a good idea to save these topics as Favorites. To save a topic as a favorite, press the Favorites tab, highlight the topic in the Topics window, and press the Add button. You can now view this topic quickly by going to the Favorites help tab.

Using th

Or, you cathe Indextopic.

Other H

To hide thicon at theview the lShow icoscreen.

To size ththe cursothe Track

To move display, pvery top oTrackball

Exiting O

To exit Onhand corn

Page 32: L3_QG_5122541_4_100

LOGI 28

Acces

To view

1. Ins2. Op3. Do

do4. Se

blu

To closright-h

NOTEAcrobaCD. O‘ar505Acroba

AccesUltras

To acc

1. LoEn

t Scanner Documentation Interface.

l to find the document, double click on the ent, and open it.

ou can search through a document, use in the Table of Contents and Index to ics, and navigate via bookmarks.

addition to viewing documentation on the d system, the Documentation CD can be ny PC.

ess the ‘X’ in the upper, right-hand corner umentation window.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

sing Documentation Via a PC

user documentation on a PC,

ert the CD into the CD drive. en the CD drive on your desktop. uble click on the ‘gedocumentation.html’ cument. lect the item you want to view (click on the e, underlined link in the File Name column).

e the window, click on the ‘X’ in the upper, and corner of the browser window.

: If your PC does not have the Adobe t Reader, the PC version is supplied on the

pen the CD and double click on enu.exe. Follow the prompts to install Adobe t Reader on your PC.

sing Documentation on the ound Scanner Via the CD-ROM

ess documentation via the CD-ROM,

gon as ‘Operator’ next to Select User Level. ter the following password: ‘uls’. Press Okay.

2. Press Utilities and insert the CD-ROM.

3. Select Scanner Utilities.

4. Selec

5. Scroldocum

NOTE: Yhyperlinkslocate top

NOTE: InUltrasounread on a

To exit, prof the doc

Page 33: L3_QG_5122541_4_100

LOGI 29

Safety

Preca

Icon d

Variou f the following flag words and icons which preced

NOTE ally:

• Ma• Us• No

s will cause:

s may cause:

or can cause:

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ution Levels

escription

s levels of safety precautions may be found on the equipment and different levels of concern are identified by one oe the precautionary statement.

: Indicates precautions or recommendations that should be used in the operation of the ultrasound system, specific

intaining an optimum system environmenting this Manualtes to emphasize or clarify a point.

DANGER Indicates that a specific hazard is known to exist which through inappropriate conditions or action

• Severe or fatal personal injury• Substantial property damage.

WARNING Indicates that a specific hazard is known to exist which through inappropriate conditions or action

• Severe personal injury• Substantial property damage.

CAUTION Indicates that a potential hazard may exist which through inappropriate conditions or actions will

• Minor injury• Property damage.

Page 34: L3_QG_5122541_4_100

LOGI 30

Haza

Potent

Usage Source

are instructionsve guidelines

ISO 7000No. 0659

back panel

of power output following easonably achievable

sthetic

ss

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

rd Symbols - Icon Description

ial hazards are indicated by the following icons:

Table 1-1: Potential Hazards

Icon Potential Hazard

BiologicalHazard

• Patient/user infection due to contaminated equipment. • Cleaning and c• Sheath and glo

Electrical Hazard

• Electrical micro-shock to patient, e.g., ventricular • Probes• ECG• Connections to

MovingHazard

• Console, accessories or optional storage devices that can fall on patient, user, or others.• Collision with persons or objects result in injury while maneuvering or during system

transport.• Injury to user from moving the console.

• Moving• Using brakes• Transporting

Acoustic Output Hazard

• Patient injury or tissue damage from ultrasound radiation. • ALARA, the usethe as low as rprinciple

Explosion Hazard

• Risk of explosion if used in the presence of flammable anesthetics. • Flammable ane

Smoke & Fire Hazard

• Patient/user injury or adverse reaction from fire or smoke.• Patient/use injury from explosion and fire.

• Replacing fuse• Outlet guideline

Page 35: L3_QG_5122541_4_100

LOGI 31

Safety

Impor

The fo user aware of particular hazards associ nal precautions may be provided throug

.

Patie

Relat

Patien

Always n entering such data. Make sure correct patien .

ns and potential hazards involving GE Medical Systems if needed.

ld result in injury.

examination.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

tant Safety Considerations

llowing topic headings (Patient Safety, and Equipment and Personnel Safety) are intended to make the equipment ated with the use of this equipment and the extent to which injury can occur if precautions are not observed. Additiohout the manual.

nt Safety

ed Hazards

t identification

include proper identification with all patient data and verify the accuracy of the patient's name or ID numbers whet ID is provided on all recorded data and hard copy prints. Identification errors could result in an incorrect diagnosis

CAUTION Improper use can result in serious injury. The user must be thoroughly familiar with the instructioultrasound examination before attempting to use the device. Training assistance is available from

The equipment user is obligated to be familiar with these concerns and avoid conditions that cou

WARNING The concerns listed can seriously affect the safety of patients undergoing a diagnostic ultrasound

Page 36: L3_QG_5122541_4_100

LOGI 32

Diagn

Equipm The equipment user must become thorou . Applications training is available through the loc nce program.

g the system to transmit acoustic output coustic output or freeze the image when

cause the transducer to build up tic output remains transmitting when the ccoustic output and freezes the image

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ostic information

ent malfunction or incorrect settings can result in measurement errors or failure to detect details within the image.ghly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctionsal GE representative. Added confidence in the equipment operation can be gained by establishing a quality assura

CAUTION The system’s acoustic output remains transmitting when the user controls are being used. Allowinwith the probe not in use (or in its holder) can cause the probe to build up heat. Always turn off anot in use.

CAUTION Allowing the machine to transmit accoustic output with the probe not in use( or in its holder) caanheat.Alwayss turn off accoustic output or freeze the image when not in use. The system’s accoususer controls are being used.The system is equiped with an auto freese feature which disables awhen the machine is not in use.

Page 37: L3_QG_5122541_4_100

LOGI 33

Safety

Relate

Mecha

The us f infection. Inspect probes often for sharp, pointe nipulating intracavity probes. Become familia

The U ugh surface damage that could cause injury o s.

.

ct with internal live parts. Inspect probes mage that could allow liquid entry.

g. Take extra care not to drop e can result in patient injury or serious

inimize exposure time and keep asonably Achievable), increasing output familiar with all controls affecting the e Manual for more information.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

d Hazards (continued)

nical hazards

e of damaged probes or improper use and manipulation of intracavity probes can result in injury or increased risk od, or rough surface damage that could cause injury or tear protective barriers. Never use excessive force when mar with all instructions and precautions provided with special purpose probes

se of damaged probes can result in injury or increased risk of infection.Inspect probes often for sharp,pointed, or ror tear protective barriers.Become familiar with all instructions and precautions provided with special purpose probe

Electrical Hazard

A damaged probe can also increase the risk of electric shock if conductive solutions come in contaoften for cracks or openings in the housing and holes in and around the acoustic lens or other daBecome familiar with the probe's use and care precautions outlined in Probes and Biopsy.

CAUTION Ultrasound transducers are sensitive instruments which can easily be damaged by rough handlintransducers and avoid contact with sharp or abrasive surfaces. A damaged housing, lens or cablimpairment or operation.

CAUTION Ultrasound can produce harmful effects in tissue and potentially result in patient injury. Always multrasound levels low when there is no medical benefit. Use the principle of ALARA (As Low As Reonly when needed to obtain diagnostic image quality. Observe the acoustic output display and beoutput level. See the Bioeffects section of the Acoustic Output chapter in the Advanced Referenc

CAUTION Do not use with Defibrillator.

This equipment does not have a defibrillator approved applied part.

CAUTION DO NOT load non-system software in system computer.

Page 38: L3_QG_5122541_4_100

LOGI 34

Trainin

It is re contact the local GE representative for trainin

ALARA basic ultrasound principles, possible biologi e ALARA principle.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

g

commended that all users receive proper training in applications before performing them in a clinical setting. Pleaseg assistance.

training is provided by GE Application Specialists. The ALARA education program for the clinical end-user coverscal effects, the derivation and meaning of the indices, ALARA principles, and examples of specific applications of th

Page 39: L3_QG_5122541_4_100

LOGI 35

Safety

Equip

Relate

proper action for the patient. Inform a

vice personnel only.

nd accessories must be securely

iagnostic ultrasound examination.

result from using an electrosurgical unit cer while operating the ESU. Where ducer is not located between the ESU

alified service personnel.unding outlet.

ins power plug. The protective earth

se the risk of shock.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ment and Personnel Safety

d Hazards

WARNING This equipment contains dangerous voltages that are capable of serious injury or death.

If any defects are observed or malfunctions occur, stop operating the equipment and perform thequalified service person and contact a Service Representative for information.

There are no user serviceable components inside the console. Refer all servicing to qualified ser

WARNING Only approved and recommended peripherals and accessories should be used. All peripherals amounted to the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 .

DANGER The concerns listed below can seriously affect the safety of equipment and personnel during a d

Explosion Hazard

Risk of explosion if used in the presence of flammable anesthetics.

CAUTION This equipment provides no special means of protection from high frequency (HF) burns that may(ESU). To reduce the risk of HF burns, avoid contact between the patient and ultrasound transducontact cannot be avoided, as in the case of TEE monitoring during surgery, make sure the transactive and dispersive electrodes and keep the ESU cables away from the transducer cable.

Electrical Hazard To avoid injury:

• Do not remove protective covers. No user serviceable parts are inside. Refer servicing to qu• To assure adequate grounding, connect the attachment plug to a reliable (hospital grade) gro• Never use any adaptor or converter of a three-prong-to-two-prong type to connect with a ma

connection will loosen.• Do not place liquids on or above the console. Spilled liquid may contact live parts and increa

• Plug any peripherals into the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 AC power outlet.

Page 40: L3_QG_5122541_4_100

LOGI 36

Relate

rmance verified by qualified service

ply circuit must be as specified in

dures. To avoid the risk of disease

ures when appropriate.ect or sterilize as needed. Refer to

y apply to personnel and equipment.

to the natural latex protein. Sensitive atex content and FDA’s March 29, 1991

e the transducer to build up heat. Always ains transmitting when the user controls

and freezes the image whenn the machin

the image when the system is not in use.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

d Hazards (continued)

CAUTION Do not use this equipment if a safety problem is known to exist. Have the unit repaired and perfopersonnel before returning to use.

Smoke & Fire Hazard

The system must be supplied from an adequately rated electrical circuit. The capacity of the supChapter 3 of the Basic User Manual.

BiologicalHazard

For patient and personnel safety, be aware of biological hazards while performing invasive procetransmission:

• Use protective barriers (gloves and probe sheaths) whenever possible. Follow sterile proced• Thoroughly clean probes and reusable accessories after each patient examination and disinf

Probes and Biopsy in the Basic User Manual for probe use and care instructions.• Follow all infection control policies established by your office, department or institution as the

CAUTION Contact with natural rubber latex may cause a severe anaphylactic reaction in persons sensitive users and patients must avoid contact with these items. Refer to package labeling to determine lMedical Alert on latex products.

CAUTION Allowing the machine to transmit acoustic output with probe not in use (or in its holder) can causturn off the acoustic output or freeze the image when not in use. The system’s acoustic output remare being used. The system is equipped with Auto Freeze feature which disables acoustic output is not in use.

CAUTION The system is equipped with an Auto Freeze feature which disables acoustic output and freezes Take care when deactivating this feature.

CAUTION Never put any device onto the monitor.

Page 41: L3_QG_5122541_4_100

LOGI 37

Safety

Relate

mended on a daily basis.

service personnel only.

anel. Touching other moving parts other

osis and monitoring.

ctro Surgicaal Unit(ESU) active and

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

d Hazards (continued)

CAUTION Archived data is managed at the individual sites. Performing data backup (to any device) is recom

CAUTION Do not unpack the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 . This must be performed by qualified

CAUTION When you move the Control Panel up/down with the monitor, place BOTH hands on the Contol Pthan the Control Panel may cause personal injury.

CAUTION Do not use the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Ultrasound system ECG wave for diagn

CAUTION To avoid skin burns in surgical use,do not place the ECG electrodes in current path between Eledispersive electrodes.Keep ESU cables away from ECG leads.

Page 42: L3_QG_5122541_4_100

LOGI 38

Devic

Label

The fo uipment.

Location

Identif See “Label Location (b)” on page 51.

Type/C

IP Cod Foot Switch

Probe connectors and PCG connector

ECG marked Type CF

Various

Inside of console

Refer to Chapter 3 in the Basic User Manual for location information.

Refer to Chapter 3 in the Basic User Manual for location information.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

e Labels

Icon Description

llowing table describes the purpose and location of safety labels and other important information provided on the eq

Table 1-2: Label Icons

Label/Icon Purpose/Meaning

ication and Rating Plate Manufacture’s name and addressDate of manufactureModel and serial numbersElectrical ratings (Volts, Amps, phase, and frequency)

lass Label Used to indicate the degree of safety or protection.

e (IPX8) Indicates the degree of protection provided by the enclosure per IEC60 529. Can be used in operating room environment.

Type BF Applied Part (man in the box) symbol is in accordance with IEC 878-02-03.

Type CF Applied Part (heart in the box) symbol is in accordance with IEC 878-02-03.

!“ATTENTION” - Consult accompanying documents” is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.

“CAUTION” - Dangerous voltage” (the lightning flash with arrowhead) is used to indicate electric shock hazards.

“Mains OFF” indicates the power off position of the mains power breaker.

“Mains ON” indicates the power on position of the mains power breaker.

Page 43: L3_QG_5122541_4_100

LOGI 39

Safety

Refer to Chapter 3 in the Basic User Manual for location information.

Internal

. Rear Panel, Cirucit breaker label of Console and Front Panel.

ECG Module

Rear of console

Rear Panel

Location

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

“ON” indicates the power on position of the power switch.CAUTION: This Power Switch DOES NOT ISOLATE Mains Supply.“Standby” indicates the power standby position of the power switch.CAUTION: This Power Switch DOES NOT ISOLATE Mains Supply.

“Protective Earth” indicates the protective earth (grounding) terminal.

~ Alternating Current. symbol is in accordance with IEC 60878-01-14

Type CF Defib-Proof Applied Part (heart in the box with paddle) symbol is in accordance with IEC 60878-02-06.

“Equipotentiality” indicates the terminal to be used for connecting equipotential conductors when interconnecting (grounding) with other equipment.

This symbol indicates that waste electrical and electronic equipment must not be disposed of as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.

Table 1-2: Label Icons

Label/Icon Purpose/Meaning

Page 44: L3_QG_5122541_4_100

LOGI 40

Class

Type o

ClDegre

TyTy

Contin

System

Footsw

*1. Cl

EQUIP ground. This additional safety precaution preven

*2. Ty

TYPE able LEAKAGE CURRENT.

*3. Ty

Type C articularly regarding allowable LEAKAGE CURR

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ifications

f protection against electric shock

ass I Equipment (*1)e of protection against electric shock

pe BF Applied part (*2) (for PCG, Probes marked with BF symbol)pe CF Applied part (*3) (for ECG, Probes marked with CF symbol)uous Operation

is Ordinary Equipment (IPX0)

itch is IPX8

ass I EQUIPMENT

MENT in which protection against electric shock does not rely on BASIC INSULATION only, but includes an earth ts exposed metal parts from becoming LIVE in the event of an insulation failure.

pe BF APPLIED PART

BF APPLIED PART providing a specified degree of protection against electric shock, with particular regard to allow

pe CF APPLIED PART

F Applied Part providing a degree of protection higher than that for TYPE BF Applied Part against electric shock pENTS.

Table 1-3: Type BF Equipment

Normal Mode Single fault condition

Patient leakage current Less than 100 microA Less than 500 microA

Table 1-4: Type CF Equipment

Normal Mode Single fault condition

Patient leakage current Less than 10 microA Less than 50 microA

Page 45: L3_QG_5122541_4_100

LOGI 41

Safety

EMC

NOTE ncy interference to other medical and non-medica plies with emissions limits for a Group 1, Class cur in a particular installation.

NOTE the user (or qualified service personnel) should

• reo• inc• po• coNOTE cables or by unauthorized changes or modific ipment.

NOTE to peripheral devices must be shielded and pr uency interference in violation of the FCC regula

NOTE ucts) in the vicinity of the equipment as it may ca ear this equipment.

The m und this equipment to fully comply with the above

EMC

All typ ransmitted through air or connecting cables ce from other equipment and at the same time n

Proper

The pr

In case

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

(Electromagnetic Compatibility)

: This equipment generates, uses and can radiate radio frequency energy. The equipment may cause radio frequel devices and radio communications. To provide reasonable protection against such interference, this product com

A Medical Devices Directive as stated in EN 60601-1-2. However, there is no guarantee that interference will not oc

: If this equipment is found to cause interference (which may be determined by turning the equipment on and off), attempt to correct the problem by one or more of the following measure(s):

rient or relocate the affected device(s)rease the separation between the equipment and the affected devicewer the equipment from a source different from that of the affected devicensult the point of purchase or service representative for further suggestions.: The manufacturer is not responsible for any interference caused by using other than recommended interconnect ations to this equipment. Unauthorized changes or modifications could void the users’ authority to operate the equ

: To comply with the regulations on electromagnetic interference for a Class A FCC Device, all interconnect cablesoperly grounded. Use of cables not properly shielded and grounded may result in the equipment causing radio freqtions.

: Do not use devices which intentionally transmit RF Signals (cellular phones, transceivers, or radio-controlled produse performance outside the published specifications. Keep the power to these types of devices turned off when n

edical staff in charge of this equipment is required to instruct technicians, patients, and other people who maybe aro requirement.

Performance

es of electronic equipment may characteristically cause electromagnetic interference with other equipment, either t. The term EMC (Electromagnetic Compatibility) indicates the capability of equipment to curb electromagnetic influenot affect other equipment with similar electromagnetic radiation from itself.

installation following the service manual is required in order to achieve the full EMC performance of the product.

oduct must be installed as stipulated in 4.2, Notice upon Installation of Product.

of issues related to EMC, please call your service personnel.

Page 46: L3_QG_5122541_4_100

LOGI 42

The m by unauthorized changes or modifications to this

Portab r networks) should be used no closer to any pa

controlled products) in the vicinity of this these type devices turned off when near

ople who may be around this equipment

ents

800 MHz - 2.5 GHz

Calcul d = [7/E1] square root of P

Where ed RF

If th be

5 5.2

20 10.5

100 24.0

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

anufacturer is not responsible for any interference caused by using other than recommended interconnect cables orequipment. Unauthorized changes or modifications could void the users’ authority to operate the equipment.

le and mobile radio communications equipment (e.g. two-way radio, cellular/cordless telephones, wireless computert of this system, including cables, than determined according to the following method:

CAUTION Do not use devices which intentionally transmit RF signals (cellular phones, transceivers, or radioequipment as it may cause performance outside the published specifications. Keep the power tothis equipment.

Keep power to these devices turned off when near this equipment.

Medical staff in charge of this equipment is required to instruct technicians, patients and other peto fully comply with the above regulation.

Table 1-5: Portable and mobile radio communications equipment distance requirem

Frequency Range: 150 kHz - 80 MHz 80 MHz - 800 MHz

ation Method: d=[3.5/V1] square root of P d = [3.5/E1] square root of P

: d= separation distance in meters, P = rated power of the transmitter, V1=compliance value for conducted RF, E1 = compliance value for radiat

e maximum transmitter power in watts is rated The separation distance in meters should

2.6 2.6

5.2 5.2

12.0 12.0

Page 47: L3_QG_5122541_4_100

LOGI 43

Safety

Notic

Separa base stations for radio (cellular/cordless) teleph predicted theoretically with accuracy. To assess d. If the measured field strength in the locatio laration, the ultrasound system should be observ e-orienting or relocating the ultrasound system

1. Us ts equipped with a power source plug sh or converter to connect with a power so

2. Lo3. Be e installation procedures (i.e. wire power

ca4. La ation manuals.

Gene

1. DeTh ising its EMC performance.Av mance of the product.

2. NoThMoa.b.c.d.

3. Op uming operation.4. Op

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

e upon Installation of Product

tion distance and effect from fixed radio communications equipment: field strengths from fixed transmitters, such asones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast transmitter cannot be the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be consideren in which the ultrasound system is used exceeds the applicable RF compliance level as stated in the immunity deced to verify normal operation. If abnormal operation is observed, additional measures may be necessary, such as r or using an RF shielded examination room may be necessary.

e either power supply cords provided by GE Medical Systems or ones designated by GE Medical Systems. Producould be plugged into the fixed power socket which has the protective grounding conductor. Never use any adaptor urce plug (i.e. three-prong-to-two-prong converter).cate the equipment as far away as possible from other electronic equipment. sure to use only the cables provided by or designated by GE Medical Systems. Connect these cables following thbles separately from signal cables).y out the main equipment and other peripherals following the installation procedures described in the Option Install

ral Notice

signation of Peripheral Equipment Connectable to This Product.e equipment indicated on Chapter 15 of the Basic User Manual can be hooked up to the product without compromoid using equipment not designated in the list. Failure to comply with this instruction may result in poor EMC perfortice against User Modificatione user should never modify this product. User modifications may cause degradation in EMC performance.dification of the product includes changes in:Cables (length, material, wiring, etc.)System installation/layoutSystem configuration/componentsSecuring system parts (cover open/close, cover screwing)

erate the system with all covers closed. If a cover is opened for some reason, be sure to shut it before starting/reserating the system with any cover open may affect EMC performance.

Page 48: L3_QG_5122541_4_100

LOGI 44

Perip

The fo OGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 to image

The LO llowing on-board image recording devices:

• Mi• So• So• Mi• HP• HPThe LO cal area network (LAN) via the rear panel Ethern

Conne ear panel.

The LO mended above if the devices and their specifi

Gener

1. Th d are used simultaneously, must be less tha

2. Th3. Th4. Ri5. E

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

heral Update for EC countries

llowing is intended to provide the users in EC countries with updated information concerning the connection of the L recording and other devices or communication networks.

GIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 has been verified for overall safety, compatibility and compliance with the fo

tsubishi CP900E/CP900UM/CP 900DW Color Video Printerny UP 895 MDW/UPD 895 B&W Video Printerny UP-21 MD/UPD21/UPD23 MD Color Video Printertsubishi P91E/P91DW B&W Printer Inkjet HP990 CXi PC Printer6122,HP5652(OFFBoard).GIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 has also been verified for compatibility, and compliance for connection to a lo

et connection, provided the LAN components are IEC/EN 60950 compliant.

ction may also be made to a CE Marked and IEC/EN 60950 compliant modem using one of the serial ports at the r

GIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 may also be used safely while connected to devices other than those recomcations, installation, and interconnection with the system conform to the requirements of IEC/EN 60601-1-1.

al precautions for installing an alternate on-board device would include:

e total power consumption of the added devices, which connect to the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 ann or equal to the rated supply of the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 .ere must be adequate heat dissipation and ventilation to prevent overheating of the device.ere must be adequate mechanical mounting of the device and stability of the combination.sk and leakage current of the combination must comply with IEC/EN 60601-1.lectromagnetic emissions and immunity of the combination must conform to IEC/EN 60601-1-2.

Page 49: L3_QG_5122541_4_100

LOGI 45

Safety

Perip

Gener

1. Th2. Sig 0601-1-1.

Decla

This sy tic environment as specified.

tions can result in an electric shock ification of compatibility and conformity to nd electromagnetic interference are the

Emi

CISPRRF Em

likely to cause any interference in nearby electronic y connected to the public low-voltage power supply rding to CISPR Class A/B.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

heral Update for EC countries (continued)

al precautions for installing an alternate off-board, remote device or a network would include:

e added device(s) must be used for their intended purpose having a compatible interface.nal or mains isolation devices and additional protective earth may be needed to assure compliance with IEC/EN 6

ration of Emissions

stem is suitable for use in the following environment. The user must assure that it is used only in the electromagne

CAUTION The connection of equipment or transmission networks other than as specified in the user instruchazard or equipment malfunction. Substitute or alternate equipment and connections requires verIEC/EN 60601-1-1 by the installer. Equipment modifications and possible resulting malfunctions aresponsibility of the owner.

Table 1-6: Declaration of Emissions

ssion Type Compliance Electromagnetic Environment

11 issions

Group 1 Class A

This system uses RF energy only for its internal function. Therefore, RF emissions are very low and are not equipment. It is suitable for use in all establishments, other than domestic establishments and those directlnetwork that supplies buildings used for domestic purposes. Note: Select only one underlined word(s) acco

Page 50: L3_QG_5122541_4_100

LOGI 46

Decla

This sy e specified guidance and only in the electro

EMC Environment and Guidance

IEC 61Static (ESD)

uld be wood, concrete, or ceramic tile. If floors are ith synthetic material, the relative humidity should 30%.er quality should be that of a typical commercial pital environment. If the user requires continued during power mains interruptions, it is ded that the system be powered from an table power source (UPS) or a Battery. is the a.c. mains voltage prior to application of the

uency magnetic fields should be at levels tic of a typical location in a typical commercial and/

environment. distance to radio communication equipment must ned according to the Table 1-5 on page 42. e may occur in the vicinity of equipment marked mbol

radation or interference may occur due to RF noise on the equipment mains power supply or l cable.Such interference of this type may delaay ation with out affecting diaqgnostic dditional mains/signal RF isolation or filtering may if this type interference occur frequently.

IEC 61Electritransie

IEC 61

IEC 61Voltagvoltag

IEC 61Powerfield

IEC 61Condu

IEC 61Radiat

NOTE nd people.If Noise generated from other electronic equipm

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ration of Immunity

stem is suitable for use in the following environment. The user must assure that the system is used according to thmagnetic environment listed.

Table 1-7: Declaration of Immunity

Immunity Type Test Level Compliance

000-4-2discharge

+ 6 KV contact

+ 8 KV air

+ 6 KV contact

+ 8 KV air

Floors shocovered wbe at leastMains powand/or hosoperation recommenuninterrupNOTE: UTtest level.Power freqcharacterisor hospitalSeparationbe maintaiInterferencwith the sy

Image degconductedother signathe examinaccuracy.Abe needed

000-4-4cal fastnt/burst

± 2 kV for mains

+ 1 KV for SIP/SOP

± 2 kV for mains

± 1 kV for SIP/SOP

000-4-5 Surge Immunity ± 1kV differential

± 2 kV common

± 1 kV differential

± 2 kV common

000-4-11e dips, short interruptions and e variations on mains supply

< 50T (> 95% dip) for 0.5 cycle;400T (60% dip) for 5 cycles;700T (30% dip) for 25 cycles;< 50T (>95% dip) for 5 sec

< 50T (> 95% dip) for 0.5 cycle;400T (60% dip) for 5 cycles;700T (30% dip) for 25 cycles;< 50T (>95% dip) for 5 sec

000-4-8 frequency (50/60 Hz) magnetic

6 A/M 6 A/m

000-4-6cted RF

3 VRMS150 kHz - 80 MHz

3 VRMS150 kHz - 80 MHz

000-4-3ed RF

3 V/m80 MHz - 2.5 GHz

3 V/m80 MHz - 2.5 GHz

: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, aent is near the probe’s center frequency,noise may appear on the image.Good power line isolation is required.

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LOGI 47

Safety

Patie

1. Pe2. Fr3. No4. Im5. Pr6. EC7. PC8. Ph9. CD

lephone Lineh

ne (AC~)ble with Protective Earth

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

nt Environmental Devices

Figure 1-1. Patient Environmental Devices

ripheral Device (Signals I/O Port, Power In)ont Panel (Signal I/O Port, Power Out)n-Imaging Probesaging Probesobe PortG CableG Sensorysio-Signal Input Panel_RW Drive

10. Rear Panel11. Power Out12. Signals I/O Port13. Footswitch Connector14. Power In15. Peripheral Devices16. Signals I/O Port17. Power In18. InSite Modem (Signal I/O Port)

19. Power Te20. Footswitc21. Power Li22. Power Ca

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LOGI 48

Accep

The de NT ENVIRONMENT.

Unap

Acces

ONMENT.

re of the requirements listed below:

oved or recommended in these

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

table Devices

vices shown in “Patient Environmental Devices” on page 1-47 are specified to be suitable for use within the PATIE

proved Devices

sories, Options, Supplies

CAUTION DO NOT connect any probes or accessories without approval by GE within the PATIENT ENVIR

See “Peripheral Update for EC countries” on page 44.

CAUTION Unapproved devices shall not be used in the patient environment.

If devices are connected without the approval of GE, the warranty will be INVALID.

Any device connected to the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 must conform to one or mo

1. IEC standard or equivalent standards appropriate to devices.2. The devices shall be connected to PROTECTIVE EARTH (GROUND).

CAUTION Unsafe operation or malfunction may result. Use only the accessories, options and supplies apprinstructions for use.

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LOGI 49

Safety

Acou

Locate al-time indication of acoustic levels being genera display is based on NEMA/AIUM Standa

Acou

The di . Although not part of the NEMA/AIUM standa on the examination and type of tissue involve

• So re increase in soft tissue.• Bo it provides an estimate of potential

tem• Cr es an estimate of potential temperature

inc

The TI ay precision is ± 0.1, and accuracy is ± 50%.

Contr

The po

The Ac

Indirec ffects portion of each control in the Modes chapte

Always

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

stic Output

d on the upper right section of the system display monitor, the acoustic output display provides the operator with reted by the system. See the Acoustic Output chapter in the Advanced Reference Manual for more information. Thisrds for Real-time Display of Thermal and Mechanic Acoustic Output Indices on Diagnostic Ultrasound Equipment.

stic Output Display Specifications

splay consists of three parts: Thermal Index (TI), Mechanical Index (MI), and a relative Acoustic Output (AO) valuerd, the AO value informs the user of where the system is operating within the range of available output. Dependingd, the TI parameter will be one of three types:

ft Tissue Thermal Index (TIS). Used when imaging soft tissue only, it provides an estimate of potential temperatune Thermal Index (TIB). Used when bone is near the focus of the image as in the third trimester OB examination,perature increase in the bone or adjacent soft tissue.

anial Bone Thermal Index (TIC). Used when bone is near the skin surface as in transcranial examination, it providrease in the bone or adjacent soft tissue.

and MI is displayed at all times. The MI and TI displays start at a value of 0.0 and increments in steps of 0.1. Displ

ols Affecting Output

tential for producing mechanical bioeffects (MI) or thermal bioeffects (TI) can be influenced by certain controls.

oustic Output control has the most significant effect on Acoustic Output.

t effects may occur when adjusting other controls. Controls that can influence MI and TI are detailed under the Bioer of the Basic User Manual.

observe the acoustic output display for possible effects.

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LOGI 50

Best p

NOTE

Acou

In orde iate scanning at a reduced default output level. T t when the system is powered on or New Patien

ct on Acoustic Output, such as Gain and

to adjust the Acoustic Output control or

ring an examination. Begin the exam with

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ractices while scanning

: Refer to the Optimization sections of the Modes chapter for a complete discussion of each control.

stic Output Default Levels

r to assure that an exam may not start at a high output level, the LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 may inithis reduced level is preset programmable and depends upon the exam category and probe selected. It takes effect is selected.

HINTS Raise the Acoustic Output only after attempting image optimization with controls that have no effeTGC.

WARNING Be sure to have read and understood control explanations for each Mode used before attemptingany control that can effect Acoustic Output.

Acoustic Output Hazard

Use the minimum necessary acoustic output to get the best diagnostic image or measurement duthe probe that provides an optimum focal depth and penetration.

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LOGI 51

Safety

Warn

Cons

objects resulting in injury to the operator.

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ing Label Locations

ole Labels

Figure 1-2. Warning Label

Figure 1-3. Warning Label Location

NOTE: Possible injury. Placing objects on top of the monitor may cause the monitor to tilt with the fallingDo not place any objects on the monitor.

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LOGI 52

Cons

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ole Labels (continued)

Figure 1-4. Label Location

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LOGI 53

Safety

Cons

1. F2. C international standard for

E3. C4. E5. V6. Id7. P8. P alified service personnel.

D controlled toy, etc. Use of these devices n e devices turned off when near this e

9. T10. E ety standards. The Mark bears the name

a ol number11. T ination.

12. W

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

ole Labels (continued)

Table 1-8: Label Location Explanations

or proper grounding, connect to hospital grade receptacle.ISPR CAUTION: The LOGIQ 3 Expert/LOGIQ 3 Pro/LOGIQ 3 conforms to the CISPR11, Group 1, Class A of thelectromagnetic disturbance characteristics. E Removed.IAJ Label (Japan).oltage Range (Indication label)/Circuit breaker and fuse.entification and Rating Plate.rescription Device (For U.S.A. Only)ossible shock hazard. Do not remove covers or panels. No user serviceable parts are inside. Refer servicing to qu

o not use the following devices near this equipment: cellular phone, radio receiver, mobile radio transimitter, radio ear this equipment could cause this equipment to perform outside the published specifications. Keep power to thesquipment.o avoid injury by tipping over, DO NOT PUSH THIS UNIT FROM THE SIDES.TL Label: ETL Listing and Certification Mark is used to designate conformance to nationally recognized product safnd/or logo of the testing laboratory, product category, safety standard to which conformity is assessed, and a contrhis machine should be used in compliance with law. Some jurisdictions restrict certain uses, such as gender determ

EEE Label.

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LOGI 54

Q 3 Expert/LOGIQ 3 Pro/LOGIQ 3 Quick Guide Direction 5122541-100 Rev. 4

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