GE Healthcare

Technical
Publications

Direction 5307393-100
Rev. 1

LOGIQ 7/LOGIQ 7 Pro

Quick Guide

R8.x.x
Copyright 2008 By General Electric Co.
Operating Documentation
Regulatory Requirement

LOGIQ 7/LOGIQ 7 Pro complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices.

This manual is a reference for the LOGIQ 7/LOGIQ 7 Pro. It applies to all versions of the R8.x.x software and later for the LOGIQ 7/LOGIQ 7 Pro
ultrasound systems.

Manufacturer

GE-Yokogawa Medical Systems, Ltd.

7-127 Asahigaoka 4-Chome, Hino-shi
Tokyo, 191-8503
JAPAN

Country-specific

MHLW: 21300BZZ00082000
SFDA REG. No: (I) 20073230515 / YZP/JAP 0004-2006

GE Healthcare

GE Medical System: Telex 3797371

P. O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)

GE Ultraschall: TEL: 49 212.28.02.208

Deutschland GmbH & Co. KG: FAX: 49 212.28.02.431
Beethovenstraße 239
Postfach 11 05 60
D-42655 Solingen GERMANY
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 A

Revision History

REV DATE REASON FOR CHANGE

1 June 27, 2008 Initial release

List of Effective Page

PAGE REVISION
NUMBER HISTORY
Title Rev. 1
A and B Rev. 1
1-56 Rev. 1

Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on ePDM/
MyWorkshop (GE Healthcare Electronic Product Data Management). If you need to know the latest revision, contact your distributor, local GE
Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at 1-800-682-5327 or 262-524-5698.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 B

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 the United States.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 1

System Power

Power On 3. Unwrap the power cable. Make sure to allow
sufficient slack in the cable so that the plug is not
To connect the system to the electrical supply: pulled out of the wall if the system is moved slightly.
1. Ensure that the wall outlet is of the appropriate type. NOTE: Use the appropriate power cord provided by
or designated by GE Medical Systems.
4. Attach the power plug to the system and secure it in
place by using the retaining clamp.
Press the Power switch to turn the power on. The circuit
breaker must also be in the on position.
The system should now go through its boot-up process
with no further user intervention (approximately 3
minutes)

Figure 1. Example Plug and Outlet Configurations a

1. 100-120 VAC, 1200 VA

a, b Plug and Outlet Configuration
2. 220-240 VAC, 1200 VA
a, b Plug and Outlet Configuration

2. Ensure that the power switch is turned off.

Figure 2. Power Plug Example

a. Retaining clamp for power plug

CAUTION: Ensure that the retaining clamp for the power
plug is fixed firmly.
5. Push the power plug securely into the wall outlet.
CAUTION: Use caution to ensure that the power cable
does not disconnect during system use. If the system is Figure 3. Power Switch Location
accidentally unplugged, data may be lost.

Preparing for an Exam

LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 2
Power Off Standby Mode Starting an Exam

To power down the system:
1. Enter the scan screen and lightly press the Power
On/Off switch at the front of the system once. The
System-Exit window is displayed.
Standby Mode pauses the system without completely
shutting down and restarting the system. This is
particularly useful for portable exams.
To activate Standby Mode,
1. Press the Power switch at the front of the system
once. The System-Exit window is displayed.
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. Using the Trackball or Tab key, select Shutdown.
The shutdown process takes about 30 seconds (the
Power On light is green) and is completed when the
control panel illumination is turned off (the Power On
light is amber).
NOTE: DO NOT select Exit for Shutdown. Exit is
only available to Service representative.
3. Disconnect the probes.
Clean or disinfect all probes as necessary. Store
them in their shipping cases to avoid damage.
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)
2. Select Standby. The monitor immediately blacks out
then press Select Patient.
while the Touch Panel and keyboard turn off.
Wait at least one minute to bring the system out of
standby mode as the system starts the standby
process after the monitor blacks out.
3. To exit Standby Mode, press and immediately
release the Power switch.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 3

Starting an Exam

New Patient Probe Selection Function Selection Window [2]

New Patient is used to clear the patient entry screen to
To start a new patient’s exam, Select a probe from the Touch Panel (the system input a new patient’s data into the database. Register is
1. Press Patient. Press the New Patient button on the automatically selects the last-used application for this used to enter new patient information into the database
Patient menu. probe). prior to the actual exam being performed. Details displays
2. Select the Exam Category. exam details and additional patient information.
Patient Entry Menu
3. Type the Patient ID, Patient Name, Birthdate, etc. EZ Backup/EZMove [3]
4. Press the Register button on the Patient menu (DO Image Management Window [1] One-step method to backup (move and delete patient
NOT press Register if you are automatically images) to an external media.
Access to this patient’s exam history and image
generating a patient ID).
management features. Dataflow [4]
5. Press Scan, B-Mode, Esc, or Exit. Select the probe
from the Touch Panel. Selects this exam’s dataflow preference.
Exit [5]
Exits the Patient Menu and returns to scanning.
Patient Information [6]
Patient ID, Name, Birthdate, Age and Sex.
Category Selection and Exam Information [7&8]
Select the appropriate category and enter the exam
information.
Patient View and Exam View [9]
Patient View lists the patients in the database. “Search
key” enables searching list by Patient ID, Last Name,
First Name, Birthdate, Sex and Last Exam date. “Search
string” and “Search from” fields help define the search
parameters.
Exam View lists the exams of the selected patient. Select
the patient or the exam in Patient View and press “Exam
View” or “Review”.

Preparing for an Exam

LOGIQ 7/LOGIQ 7 Pro Quick Guide
LOGIQ 7/LOGIQ 7 Pro Control Panel Tour
1. Touch Panel. Touch the Touch Panel to adjust
controls.
At the bottom of the Touch Panel, there are five
combination rotary dials/push buttons. The
functionality of these keys changes, depending upon
the currently displayed menu. Press the button to
switch between controls (as with Focus Position/
Number), or rotate the dial to adjust the value.
2. Touch Panel Brightness. Rotate to adjust.
3. Video. Press to control the VCR/DVR.
4. Audio Volume. Press to turn microphone on/off;
rotate to adjust speaker volume.
5. TGC. Move slide pots left/right to adjust TGC.
6. Reverse. Press to invert the image left/right.
15
14
4 11
7
8 10
Control Panel/
Touch Panel Tour
Direction 5307393-100 Rev. 1 4
7. Additional Feature Keys. Patient, LOGIQView, 3D/ 13. Freeze and Print Keys. Press Freeze to
4D, Contrast, Harmonics. Press to activate these freeze the image; press the P keys to archive, print,
controls. or send the image.
8. Keyboard. Use the keyboard to enter patient 14. Probe Holder.
information and annotations. 15. Gel Holder.
9. Mode/Gain Keys: Press these key to activate the
mode; rotate the key to adjust the Gain.
10. Imaging/Measurement Keys: Clear, Comment, Body
Pattern, Ellipse, Measure, Zoom, M/D Cursor, Scan
Area, Set. Press or rotate these keys, as necessary.
11. Depth. Rotate to adjust the Depth.
12. Imaging Feature Keys: Auto Optimize On/Off, B
Pause, Multi Image Left/Right Select. Press these
keys to activate/deactivate these functions.
2 1 5
15
6
14
13
9 12
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 5

LOGIQ 7/LOGIQ 7 Pro Touch Panel Tour

In general, the key name is indicated at the top of the key. 5. Press knob below the Touch Panel to select
There are different types of Touch Panel keys: additional control, then rotate the knob to set values.
1. Press to toggle control on/off. 6. Press to move to the next Touch Panel page.
2. Progression keys are used to assess the impact of
the control on the image progressively.
3. Progress/Select keys are used for controls that have
three or more choices.
4. Rotate the knob below the Touch Panel to set values.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 6
LOGIQ 7/LOGIQ 7 Pro Monitor Display Tour
1. Institution/Hospital Name, Date, Time, Operator 10. Measurement. 20. Current date/time, Caps Lock (lit when on), network
Identification. 11. Measurement Results Window. connection indicator (PC=connected, PC with X=not
2. Patient Name, Patient Identification. 12. Probe Identifier. Exam Study. connected, Human Face (VoiceScan), System
3. Acoustic Output Readout Messages display.
13. Imaging Parameters by Mode.
4. GE Symbol (Probe Orientation Marker). The symbol 21. Trackball Functionality Status: Scroll,
14. Focal Zone.
is reversed on flipped images. M&A (Measurement and Analysis), Position, Size,
15. TGC. Scan Area Width and Tilt.
5. Image Preview, zoom reference box. 16. Body Pattern.
6. Gray/Color Bar. 17. Depth Scale.
7. Cine Gauge. CINE frame/Total # of CINE frames (28/ 18. Image Management Menu: Active Images, Delete,
51), Frame time/total loop time. Previous/Next Image and Menu.
8. Measurement Summary Window. 19. Image Clipboard.
9. Image.

Control Panel/
Touch Panel Tour
LOGIQ 7/LOGIQ 7 Pro Quick Guide
B/M-Mode Image Optimize
Power Output
Optimizes image quality and allows user to reduce beam
intensity. 2% increments between 0-100%. Values greater
than 0.1 are displayed.
Dynamic Range
Dynamic Range controls how echo intensities are
converted to shades of gray, thereby increasing the
adjustable range of contrast.
Focus
Increases the number of focal zones, moves the focal
zone(s), and changes the zone width, so that you can
tighten up the beam for a specific area. A graphic caret
corresponding to the focal zone position(s) appears on
the right edge of the image.
NOTE: Push key to toggle between Focus Number and
Focus Position.
Virtual Convex
On Linear and Sector probes, provides a larger field of
view in the far field.
Rejection
Selects a level below which echoes will not be amplified
(an echo must have a certain minimum amplitude before
it will be processed).
Frame Average
Temporal filter that averages frames together. This has
the effect of presenting a smoother, softer image.
CrossXBeam and CrossXBeeam#(Option)
CrossBeam combines multiple co-planar images from
different view angles into a single image at real-time
frame rates, using bi-cubic interpolation.
Direction 5307393-100 Rev. 1 7
SRI-HD (Option) B Softener
SRI-HD (High Detection Speckle Reduction Imaging) is Affects amount of lateral smoothing.
an adaptive algorithm to reduce the unwanted effects of
speckle in the ultrasound image. Suppression
Eliminates low-level echoes associated with
B Steer
acoustic/electrical noise.
You can slant the B-Mode or Color Flow linear image left
or right to get more information without moving the probe. Focus width
The angle steer function only applies to linear probes.
To change the zone width, use Focus Width on the B-
Mode Touch Panel page 2.
Edge Enhance
Edge Enhance brings out subtle tissue differences and Range Focus
boundaries by enhancing the gray scale differences
Improves the near/mid field image quality, borders/
corresponding to the edges of structures. Adjustments to
interfaces, increases contrast and detail resolution across
M Mode's edge enhancement affects the M Mode only.
the image, and allows for less filling in the vessels.
Colorize
Diff
Enables gray scale image colorization. To deactivate,
Reduces noise artifacts in the image. When you activate
reselect a Gray Map.
Diff, the frame rate decreases and the noise artifacts are
filtered.
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.
Coded Excitation (CE)
Improves image resolution and
penetration in the far field.
Frequency
Multi Frequency mode lets you downshift to
the probe's next lower frequency or shift up
to a higher frequency.
Line Density
Optimizes B Mode frame rate or spatial
resolution for the best possible image.
LOGIQ 7/LOGIQ 7 Pro Quick Guide
B/M-Mode Image Optimize (continued)
Anatomical M-Mode
Allows you to rotate or move the M line in order to image
difficult-to-reach anatomy.
Curved Anatomical M-Mode (CAMM)
Displays a distance/time plot from a free-drawn cursor
line.
Sweep Speed
Changes the speed at which the timeline is swept.
Full Timeline
Expands display to full timeline display.
Display Format
Changes the horizontal/vertical display layout between B-
Mode and M-Mode.
B-Flow (Option)
Provides a more intuitive representation of non-
quantitative hemodynamics in vascular structures.
Sensitivity/PRI: Adjusts the sample rate for the flow
signal.
Background On/Off: Background On views the
anatomy roadmap; Background Off views flow
information only.
Direction 5307393-100 Rev. 1 8
B/M-Mode Control Panel Controls Frequency. Changes system parameters to best
optimize for a particular patient type.
Auto Optimize Maps. There is an inter-dependency between gray maps,
gain, and dynamic range. If you change a map, revisit
Automatic Tissue Optimization optimizes the image
gain and dynamic range settings.
based upon a specified Region of Interest (ROI) or
Dynamic Range. Affects the amount of gray scale
anatomy within the display.
information displayed.
Zoom Edge Enhance. Better delineates the amount of border
Magnifies a zoom region of interest, which is magnified to sharpness.
approximately the size of a full-sized image. An un-
Frame Average. Smooths the image by averaging
zoomed reference image is displayed adjacent to the
frames. Affects the amount of speckle reduction.
zoom window. The system adjusts all imaging parameters
accordingly. Press to activate/deactivate; rotate to
increase/decrease zoom factor. Use the Trackball to
position the Zoom ROI.
Reverse
Flips the image left/right. The GE symbol flips
accordingly.
Multi Image
Press L to activate Multi Image; press R/L to toggle
between live image.
B/M Mode Scanning Hints
Auto Optimize. Improves imaging
performance while reducing optimization
time.
Coded Harmonics. Enhances near field
resolution for improved small parts and
OB/GYN imaging as well as far field
penetration.
B/M Mode
Image Optimize
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 9

Color Flow/Doppler Image Optimize

Angle Correct Invert Trace Method

Estimates the flow velocity in a direction at an angle to Allows blood flow to be viewed from a different Specify Max, Mean, or Off.
the Doppler vector by computing the angle between the perspective, i.e. red away (negative velocities) and blue
Doppler vector and the flow to be measured. toward (positive velocities). The real-time or frozen image Spatial Filter
can be inverted. Smooths out the color, makes it look less pixely.
Angle Steer/Fine Angle Steer
Angle Steer slants the Color Flow region of interest or the Packet Size Duplex
Doppler M line to obtain a better Doppler angle. Controls the number of samples gathered for a single Duplex on: simultaneous B+CF+PW(CW) mode started in
color flow vector triplex mode.; Duplex off: Toggle via live B+CF and
Press Angle Steer to access Fine Angle Steer. Fine Angle
Steer allows you to steer the Doppler cursor left/right 5, PW(CW) mode via B-Pause.
Accumulation
10, 15 and 20 degrees. Available from the Doppler Mode
Touch Panel. Enhances the flow in an image. Map Compress
When you increase the value, high velocity elements in
Baseline Modify Auto Calcs the map are compressed so that the map darkens. When
Adjusts the baseline to accommodate faster or slower Press to select desired Auto Calcs. you decrease the value, low velocity elements in the map
blood flows to eliminate aliasing. are compressed so that the map lightens. The effect is
Trace Sensitivity visible in the color bar.
PRF/Wall Filter In Auto Calcs, increase to pick up more signal or
Velocity scale determines pulse repetition frequency. If decrease to pick up less signal.
the sample volume gate range exceeds single gate PRF
capability, the system automatically switches to high PRF Trace Direction
mode. Multiple gates appear, and HPRF is indicated on Select Above, Below, or Both.
the display.
Wall Filter insulates the Doppler signal from excessive Auto Calcs
noise caused from vessel movement. Specify Auto Calcs Off/Live/Frozen.
NOTE: Push key to toggle between PRF and Wall Filter.
Quick Angle
Threshold Quickly adjusts the angle by 60 degrees.
Threshold assigns the gray scale level at which color
Sample Volume Gate Length
information stops.
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.
LOGIQ 7/LOGIQ 7 Pro Quick Guide
Color Flow/Doppler Image Optimize (continued)
PW/CF Ratio
The PW/CF Ratio is active when “Depend Triplex” is on in
triplex mode. It is used to set the PRF ratio between PW
and CFM.
Compression
Increase to make frozen image appear more contrasty;
decrease to make frozen image appear softer.
Time Resolution
Lower makes the image appear smoother; higher makes
the image appear sharper.
Flash Suppression
Activates/deactivates Flash Suppression, a motion
artifact elimination process.
Color Flow Control Panel Control
Scan Area. Toggles between the CFM ROI window size
and position.
M/D Cursor. Activates the Doppler cursor.
PFD Mode (Option. LOGIQ 7 only). PFD Mode shows
pulsation of a flow superimposed on a PDI or Directional
PDI image. Using PFD, you can differentiate between
pulsatile flow in the liver arteries (green) and non-pulsatile
flow in the Portal vein at one glance. Flow existence, flow
direction and vasculature information are available.
PDI Mode is a color flow mapping technique used to map
the strength of the Doppler signal coming from the flow
rather than the frequency shift of the signal.
Direction 5307393-100 Rev. 1 10
Continuous Wave Doppler To decrease motion artifact. Increase the PRF, and
increase the Wall Filter.
Allows examination of blood flow data all along the
To eliminate aliasing. Increase the PRF and lower the
doppler cursor rather than from any specific depth.Gather
Baseline.
samples along the entire Doppler beam for rapid
scanning of the heart. Range gated CW allows Line Density. Trades frame rate for sensitivity and spatial
information to be gathered at higher velocities. resolution. If the frame rate is too slow, reduce the size of
the region of interest, select a different line density
There are two CW Doppler operating modes:
setting, or reduce the packet size.
Steerable - Allows viewing of the B-Mode image to
For venous imaging. Ensure that you have selected the
position the Doppler cursor to the area of interest while
vascular exam category, select a venous application,
viewing the Doppler Spectrum (shown below the B-mode
select the appropriate probe for very superficial structure,
image) and listening to the Doppler audio signal. Works
select two focal zones, adjust the depth to the anatomy to
with only Sector Probes.
be imaged, maintain a low gain setting for gray scale,
Non-Imaging - Provides only Doppler Spectrum and activate Color Flow, maintain the PRF at a lower setting,
Audio for ascending/descending aortic arch, other hard- and increase Frame Averaging for more persistence.
to-get-to spaces or higher velocities. Requires a single
CWD probe and adapter. Works with only CWD Probes
(P2D and P6D).
Scanning Hints
Wall Filter. Affects low flow sensitivity versus motion
artifact.
To improve sensitivity. Increase Gain,
decrease PRF, increase Power Output,
adjust Line Density, decrease Wall Filter,
increase Frame Averaging, increase
Packet Size, reduce ROI to the smallest
reasonable size, and position the Focal
Zones properly.
Color Flow/Doppler Mode
Image Optimize
LOGIQ 7/LOGIQ 7 Pro Quick Guide
Basic Measurements
NOTE: The following instructions assume that you first
scan the patient and then press Freeze.
Distance and Tissue Depth Measurements
1. Press Measure once; an active caliper displays.
2. To position the active caliper at the start point
(distance) or the most anterior point (tissue depth),
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 active caliper at the end point
(distance) or the most posterior point (tissue depth),
move the Trackball.
5. To complete the measurement, press Set. The
system displays the distance or tissue depth value in
the measurement results window.
NOTE: 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.
NOTE: To rotate through and activate previously fixed
calipers, turn Cursor Select.
NOTE: After you complete the measurement, to erase
all data that has been measured to this point, but not data
entered onto worksheets, press Clear.
Direction 5307393-100 Rev. 1
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.
11
Circumference/Area (Trace) Measurement
1. Press Measure twice; a trace caliper displays.
2. To position the trace caliper at the start point, move
the Trackball.
3. To fix the trace start point, press Set. The trace
caliper changes to an active caliper.
4. To trace the measurement area, move the Trackball
around the anatomy. A dotted line shows the traced
area.
NOTE: To erase the dotted line but not the trace caliper,
press Clear once. To clear the trace caliper and the
current data measured, press Clear twice.
NOTE: To erase the line (bit by bit) back from its current
point, move the Trackball or turn the Ellipse control
counterclockwise.
5. To complete the measurement, press Set. The
system displays the circumference and the area in
the measurement results window.
NOTE: Before you complete a measurement:
To erase the line (bit by bit) back from its current
point, move the Trackball or turn the Ellipse
control counterclockwise.
To erase the dotted line but not the trace caliper,
press Clear once.
To clear the trace caliper and the current data
measured, press Clear twice.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 12
Circumference and area (Spline trace) Echo Level measurement
measurement To make an echo level measurement;
To trace the circumference of a portion of the anatomy 1. Press Measure three times to enable the echo level
and calculate its area: measurement. A trace caliper displays.
1. Press Measure twice; a trace caliper displays. 2. To position the trace caliper at the start point, move
2. To position the first caliper at the start point, move the Trackball.
the Trackball. 3. To fix the trace start point, press Set. The trace
3. To fix the trace start point, press Set. The first caliper caliper changes to an active caliper.
becomes yellow and the second caliper appears at 4. To trace the measurement area, move the Trackball
the same position as the first caliper and is green. around the anatomy. A dotted line shows the traced
NOTE: When pressing the Clear key once, the area.
second caliper disappears and the first caliper is 5. To complete the measurement, press Set. The
activated. system displays the echo level in the Results
If Clear is pressed again, the first caliper disappears Window.
and the Spline trace is cancelled. NOTE: The echo level measurement is only available
4. To position the second caliper, move the Trackball on a frozen image, not on a B-paused image.
and press Set. The third caliper appears at the same
position.
NOTE: The Clear key functionality is the same as
noted in the previous step.
The spline trace requires at least three points to draw
the trace. Continue setting the points of the trace
until the desired points are set.
To position the 1st caliper at the start point, move the
Trackball.
5. Press Set again after the last caliper is fixed to
finalize the spline trace. All points are removed from
the line and the spline trace turns yellow.
Press Set twice to finish this measurement.
If Clear is pressed twice when more than 3 points
exist on the trace, all points are removed and the first
caliper again displays.
NOTE: Spline trace is not available through the factory
default. The system defaults to trace.

Basic Measurements/
Calculations
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 13

Volume Velocity Measurement Worksheets

1. To make a volume calculation, do one of the
following:
• Make one distance measurement.
• Make two distance measurements.
• Make three distance measurements.
NOTE: Three distances should be done in the dual
format mode (side by side images). One
measurement is usually made in the sagittal plane
and two measurements in the axial plane.
• Make one distance and one ellipse measurement.
• Make one ellipse measurement.
2. Select Volume.
Time Interval Measurement
1. Press Measure twice; and active caliper with a
vertical dotted line displays.
2. To position the active caliper at the start point, 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 at the end point, move
the Trackball.
5. To complete the measurement, press Set. The
system displays the time interval between the two
calipers in the measurement results window.
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, PS/ED Ratio, ED/PS Ratio or A/B Ratio
Select PI, RI, PS/ED Ratio, A/B Ratio or ED/PS Ratio
from the Doppler Touch Panel. 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 PS/ED ratio, “A” velocity for A/B
ratio or diastole for ED/PS 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 PS/ED ratio,
“B” velocity for A/B ratio or systole for ED/PS 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.
Measurement/Calculation worksheets are available to
display and edit measurements. There are generic
worksheets as well as Application specific worksheets.
The worksheets are selected from the Measurement
Touch Panel.
Reports
The system enables the generation of patient reports,
based on the examination performed and the analyses
that were made during examinations. The reports are
generated using the data stored in the system with pre-
selected templates.
For more information, see the LOGIQ 7/LOGIQ 7 Pro
Basic User Manual Chapter 14 “ReportWriter”.
Activating the report
1. Select Report on the Touch Panel. Report page is
displayed.
2. Select the desired application and template by
TEMPLATE.
3. Edit the report as necessary.
• Change the Patient Data
• Insert the images or anatomical graphics.
• Type the examiner’s comment, etc.
4. Print the report as necessary.
5. Select Store to save the report. Select another key to
close the report.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 14
Using Probes

Connecting a probe Deactivating the probe

1. Place the probe's carrying case on a stable surface When deactivating the probe, the probe is automatically
and open the case. placed in standby mode.
2. Carefully remove the probe and unwrap the probe Press the Freeze key or select another probe.
cable.
3. DO NOT allow the probe head to hang free. Impact Disconnecting the probe
to the probe head could result in irreparable damage.
Probes can be disconnected at any time. However, the
4. Turn the connector locking handle clockwise. probe should not be selected as the active probe.
5. Align the connector with the probe port and carefully 1. Move the probe locking handle counterclockwise.
push into place. Pull the probe and connector straight out of the
6. Turn the connector locking handle clockwise to probe port.
secure the probe connector. 2. Carefully slide the probe and connector away from
7. Carefully position the probe cable in the probe cord the probe port and around the right side of the
holder spot so it is free to move, but not resting on keyboard. Ensure the cable is free.
the floor. 3. Be sure that the probe head is clean before placing
the probe in its storage box.
Activating the probe
Select the appropriate probe from the probe indicators on
the Touch Panel.
The probe activates in the currently-selected operating
mode. The probe's default settings for the mode and
selected exam are used automatically.

Using Probes
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 15

Probe Application
Table 1: Probe Indications for Use

Probe
Application 3C 3.5C 3.5CS 4C 5C 8C M7C* E8C BE9C 3CRF 7L 9L 10L 11L 12L i12L M12L T739

Abdomen X X X X X X X X

Small Parts X X X X X X X X

Periph. Vasc. X X X X X X X 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 X

Neonatal X X X X

Urology X X X X X X X X

Surgery X X

Cardiac

Transcranial

Transesophageal

Transvaginal X

Transrectal X X

* LOGIQ 7 only

NOTE: Probes for transvaginal, transrectal and transesophageal applications require special handling. Refer to the user documentation enclosed with these probes.
NOTE: Not all probes described in this document may be available or cleared for sale in all markets.

CAUTION

Check the temperature of the room before you use the 4D probe. Use the 4D probe at temperatures of 30 degrees C (86 degrees F) or lower.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 16
Probe Application (continued)

Table 2: Probe Indications for Use

Probe
Application 3S 7S 10S M3S 6T P2D P6D 4D10L 4D3C-L 4DE7C

Abdomen X X X X X

Small Parts X X

Periph. Vasc. X X

Obstetrics X X

Gynecology X X

Pediatrics X X X X X

Neonatal X

Urology

Surgery

Cardiac X X X X X X

Transcranial X X

Transesophageal X

Transvaginal X

Transrectal X

CAUTION

NOTE: Check the temperature of the room before you use the 4D probe. Use the 4D probe at temperatures of 30 degrees C (86 degrees F) or lower

Using Probes
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 17

Probe Features
Table 3: Probe Features

Probe Feature 3C 3.5C 3.5CS 4C 5C 8C M7C* E8C BE9C 3CRF 7L 9L 10L 11L 12L i12L M12L T739

Coded Excitation X

Coded Harmonics X X X X X X X X X X X X X X X X X

B-Flow X X X X X X X X X X X X

SRI-HD X X X X X X X X X X X X X X X X X X

Coded Contrast X X X X X X X X

LOGIQ View X X X X X X X X X X X X X X X X X X

Virtual Convex X X X X X X X X

Easy 3D X X X X X X X X X X X X X X X X X X

Advanced 3D X X X X X X X X X X X X X X X X X X

Volume 3D/4D

Anatomical M X X X X X X X X X X X X X X X X X X

TruAccess X X X X X X X X X X X X X X X X X X

Biopsy X X X X X X X* X X X X X X X X

PFD X X X X X X X X X X X X X X X X X X

TVI

CrossXBeam X X X X X X X X X X X X X X X X

PDI X X X X X X X X X X X X X X X X X X

CW

* LOGIQ 7 only

NOTE: E8C offers disposable or reusable biopsy guides.

LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 18
Probe Features
Table 4: Probe Features

Probe Feature 3S 7S 10S M3S* 6T P2D P6D 4D10L 4D3C-L 4DE7C

Coded Excitation

Coded Harmonics X X X X X X X

B-Flow X X X

SRI-HD X X X X X X X X

Coded Contrast X X X

LOGIQ View X X X X X X X X

Virtual Convex X X X X X X

Easy 3D X X X X

Advanced 3D X X X X

Volume 3D/4D X X X

Anatomical M X X X X X X X X

TruAccess X X X X X X X X

Biopsy X X X X X

PFD X X X X X X X

TVI X X X X X

CrossXBeam X X X

PDI X X X X X X X X

CW X X X X X X X

Using Probes
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 19

Probe Cleaning and Disinfection Instructions

Probe Safety
Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use care when handling and protect from damage when not in
WARNING
use. DO NOT use a damaged or defective probe. Failure to follow these precautions can result in serious injury and equipment damage.

Ultrasound transducers can easily be damaged by improper handling and by contact with certain chemicals. Failure to follow these precautions can result in serious injury
and equipment damage.
• Do not immerse the probe into any liquid beyond the level specified for that probe. Never immerse the transducer connector or probe adapters into any liquid.
• 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 hydrogen peroxide
• 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 damaged or defective probe.

Adequate cleaning and disinfection are necessary to prevent disease transmission. It is the responsibility of the equipment user to verify and maintain the effectiveness of the
CAUTION
infection control procedures in use. Always use sterile, legally marketed probe sheaths for intra-cavitary and intra-operative procedures.

For neurological intra-operative procedures, use of a legally marketed, sterile, pyrogen free probe sheath is REQUIRED. Probes for neuro surgical use must not be sterilized
with liquid chemical sterilants because of the possibility of neuro toxic residues remaining on the probe.
Biological
Hazard 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 intercavitary probes.
• Inspect probes for sharp edges or rough surfaces that could injure sensitive tissue.
• DO NOT apply excessive force to the probe connector when inserting into the probe port. The pin of a probe connector may bend.

In order for liquid chemical germicides to be effective, all visible residue must be removed during the cleaning process. Thoroughly clean the probe, as described on the
following 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 disinfecting means.

Electrical The probe is driven with electrical energy that can injure the patient or user if live internal parts are contacted by conductive solution:
• DO NOT immerse the probe into any liquid beyond the level indicated by the immersion level diagram. Never immerse the probe connector or probe adaptors into any liquid.
Hazard • DO NOT drop the probes or subject them to other types of mechanical shock or impact. Degraded performance or damage such as cracks or chips in the housing may
result.
• Inspect the probe before and after each use for damage or degradation to the housing, strain relief, lens, and seal. A thorough inspection should be conducted during the
cleaning process.
• Before inserting the connector into the probe port, inspect the probe connector pins. If a pin is bent, do not use the probe until it has been inspected and repaired/replaced
by a GE Service Representative.
• 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 the service manual for leakage check procedures.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 20
Probe Cleaning, After Each Use Probe Immersion Levels You MUST disconnect the probe from the LOGIQ 7/
LOGIQ 7 Pro prior to cleaning/disinfecting the probe.
1. Disconnect probe from ultrasound console and
Failure to do so could damage the system.
remove all coupling gel from probe by wiping with a M7C 8C
BE9C
3C
E8C
soft cloth and rinsing with flowing water. 3.5C
3.5CS
5C
Probe Disinfection Agents
2. Wash the probe with mild soap in lukewarm water. 4D 10L 4D 3C-L

Scrub the probe as needed using a soft sponge, Ultrasound probes can be disinfected using liquid
gauze, or cloth to remove all visible residue from the chemical germicides. The level of disinfection is directly
probe surface. Prolonged soaking or scrubbing with related to the duration of contact with the germicide.
a soft bristle brush (such as a toothbrush) may be Increased contact time produces a higher level of
necessary if material has dried onto the probe 10S disinfection.
4C
3S
surface. M3S
7S
P2D
P6D Refer to the Probe Care Card. To view the probe care
4DE7C
3. Rinse the probe with enough clean potable water to cards online, the website is the following:
remove all visible soap residue.
6T http://www.gehealthcare.com/usen/ultrasound/products/
4. Air dry or dry with a soft cloth. probe_care.html
i12L
7L 9L
Probe Disinfection, After Each Use 10L
12L
11L
M12L
T739
CAUTION
1. Prepare the germicide solution according to the
manufacturer's instructions. Be sure to follow all
precautions for storage, use and disposal. Take extra care to handling the lens face of the
2. Place the cleaned and dried probe in contact with the Ultrasound transducer. The lens face is especially
germicide for the time specified by the germicide 3CRF sensitive which can easily be damaged by rough
manufacturer. High-level disinfection is handling. Never use excessive force when cleaning the
recommended for surface probes and is required for 1 2 3
lens face.
endocavitary and intraoperative probes (follow the
germicide manufacturer's recommended time).
Probes for neuro surgical intra-operative use must
NOT be sterilized with liquid chemical sterilants NOTE: * LOGIQ 7 only.
because of the possibility of neuro toxic residues 1. Fluid Level
remaining on the probe. Neurological procedures
2. Aperture
must be done with the use of legally marketed,
sterile, pyrogen free probe sheaths. 3. Contact face within patient environment
3. After removing from the germicide, rinse the probe
following the germicide manufacturer's rinsing CAUTION
instructions. Flush all visible germicide residue from
the probe and allow to air dry.

In order for liquid chemical germicides to be effective, all

visible residue must be removed during the cleaning
process. Thoroughly clean the probe, as described earlier
before attempting disinfection.

Using Probes
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 21

Image Management

Clipboard Formatting a storage medium Backing Up Patient Information

As images are saved by pressing any of the print keys
(P1, P2, P3, or P4), the images appear at the bottom of
the display on the clipboard as thumbnails of the images
saved during the exam. These images remain on the
clipboard until the end of the exam.
Printing Images
Press the appropriate print key (P1, P2, P3, or P4). For
more information on programming the Print buttons, See
“Dataflow” on page 25.
Browsing an Exam’s Stored Images
‘Mouse over’ the image in the clipboard, then press Set to
view an enlarged thumbnail image.
Managing an Exam’s Stored Images
From the Display, press Active Images; from the Patient
menu, open Active Images.
Deleting an Image
Select the image on the clipboard, then press the
onscreen Delete shortcut.
Or, go to Active Images (lower, right-hand portion of the
display). Highlight all the images that need to be deleted
and press Delete All Temp Images from the Touch
Panel.
1. Insert the backup media. Format the backup media. Format a medium prior to following these steps.
Select Utility -> Connectivity -> Removable media
1. Select the Utility -> System, then Backup/Restore
tab. Select the media type. Label the media
tab.
appropriately. Press Format.
2. Select the media.
Storage media: CD-R, DVD-R, DVD-RAM (non-
cartridge and disk removable cartridge) and USB
Flash Drive.
CAUTION DO NOT use DVD-RW, DVD+R
and CD-RW and DVD-RAM (disk
non-removable cartridge). The
LOGIQ 7/LOGIQ 7 Pro does not
support these media.
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.
3. Select the parameter under Backup by placing a
check mark. Then press Backup.
4. Answer ‘OK’ to the Back-Up pop-up message.
NOTE: The detailed section of this menu decouples the
user defined configuration above. This allows you to
selectively restore what you want to restore across
multiple machines.

Image/ Patient Management

and Connectivity
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 22
Moving Data Between Ultrasound Systems
There are 5 options (Import, Export, Q/R, Worklist and Query/Retrieve (Q/R) Send To the DICOM device
MPEGvue) under Data Transfer.
1. Press Patient and select Data Transfer. 1. Press Patient.
Import 2. Select Q/R. The local archive is enabled for the 2. Search and select the patient and press Exam. The
transfer process. Patient Exam screen displays.
1. At the other Ultrasound system, insert the removable
3. Select the Query/Retrieve server from the Transfer 3. Select the exam which has the images and press
media.
From pull-down menu. Send To.
2. Press Patient and select Data Transfer.
4. Press Query in the Transfer From section. The NOTE: You can only select the Local Archive-Int.
3. Select Import. server’s patient list displays. HD for Workflow.
4. Select the media from the Transfer From pull-down 5. Select the patient(s) or exam(s) to retrieve from the 4. The Send To dialogue box displays. Choose the
menu. patient list. destination device and select OK.
5. Select the patient(s) or exam(s) from the Transfer 6. Press Transfer. The data is retrieved from the server NOTE: The destination device is configured in the
From Search field for import. as the progress bar displays. Utility screen. Multiple devices are able to be
6. Press Transfer. configured.
7. Wait until the patient information is copied and press Worklist
F3 when finished to eject the media. 5. The successful/unsuccessful message is displayed
1. Press Patient and select Worklist. at the bottom of the screen.
2. The last Worklist used displays on the monitor.
Export NOTE: If you press the Clear button in the Transfer
3. Press Refresh to refresh the list or select another From and Transfer To section, all the search criteria is
1. Press Patient and select Data Transfer. Worklist server from the transfer From pull-down cleared and the list is refreshed accordingly.
2. Select Export. menu.
3. Select the patient(s) or exam(s) to export in the 4. Select the patient(s) or exam(s) from the list.
Transfer From Search field (the top portion). 5. Press Transfer. The progress bar displays during the
4. Select the destination at the Transfer To pull-down transfer.
menu.
5. Press Transfer. The progress bar displays during the MPEGvue
transfer. Save the data to the media to view on PC
6. Press F3 to eject the media. Specify that you want to
finalize the CD-R or DVD-R. 1. Format and label the media. Or insert the USB Flash
Drive or USB HDD into the USB Port.
2. Press Patient and select Data Transfer.
3. Select MPEGvue. The patient list in the Local
Archive-Int. HD displays in the Transfer From
section.
4. Select the media or USB Flash Drive from the
Transfer To pull-down menu.
5. Select the patient(s) or exam(s) from the list.
6. Press Transfer. The progress bar displays during the
transfer.
LOGIQ 7/LOGIQ 7 Pro Quick Guide
EZBackup/EZMove
EZBackup/EZMove allows you to backup the patient
database and images.
1. To start the EZBackup/EZMove procedure, go to the
Patient menu and press the EZBackup or EZMove
button. The EZBackup/EZMove Wizard starts.
NOTE: EZBackup/EZMove can take up to 20 minutes.
Make sure to schedule this at the same time daily, when
no patients are scheduled.
2. Verify the information on the first page of the
EZBackup/EZMove Wizard, then press Next.
NOTE: If the EZBackup/EZMove presets need to be
modified, those requirements are specified on the Utility -
-> System --> Backup/Restore page.
3. Verify the information on the EZBackup/EZMove
Wizard, Page 2. This page tells you how many
medias you need to do this backup. After you have
gathered the media, you are ready to begin the
backup. Press Next.
4. A pop-up message appears that provides you with
the media label. Label the media, then insert 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
Label the media, then insert the media and press OK.
6. When the backup is complete, the Backup
completed page appears.
Image/ Patient Management
and Connectivity
Direction 5307393-100 Rev. 1
SaveAs
Format a medium prior to following these steps.
1. Insert the media into the drive.
NOTE: If you have not formatted the media, the
media will be formatted when you select Save As.
2. On the scan screen, press the left Set key. The arrow
cursor displays.
3. Place the cursor on the image or CINE Loop in the
clipboard to be saved and press Set. The image
displays on the screen.
4. Select Menu in the lower, right-hand corner of the
screen. The system menu displays.
NOTE: If you save the image as an.avi file, run the
CINE Loop before you select Menu.
NOTE: You can not save 2D cineloop image as a
.jpeg file.
5. Select Save As. The SAVE AS menu appears.
6. Select the media from the Save in Archive pull-down
menu.
7. Folder name: You can create the folder for the saved
file.
8. File Name: The name of the file is automatically filled
in, but you can change the file name in the File name
field.
NOTE: DO NOT use the special characters.
9. Store: Select Image only or Secondary capture.
• Image only: Saves only the ultrasound image
area
• Secondary capture: Saves the ultrasound image
area, title bar, and scan information area. Not
available for DICOM or RawDICOM images.
10. Compression: Specify Compression.
• None / Rle / Jpeg / Lossless-Jpeg
11. Quality: Specify image quality (between 10-100). A
high quality setting gives a lower compression.
12. Save as type: Select one of the following.
• RawDICOM: saves the still image or CINE Loop
in both GE raw format and DICOM format.
23
• DICOM: saves the still image or CINE Loop in
pure DICOM format.
• AVI: Saves the CINE Loop in avi format.
• JPEG: Saves the still image in jpeg format.
• WMV: Saves the CINE Loop in wmv format
If you want to see all data you save into HDD, select
“AllFiles(.*)”. All the data names display in the
window.
NOTE: Save button is disabled when you select
“AllFiles”. Select each Save as type when you want
save data.
13. Press Save.
The images are saved directly to the USB drives or
Network storage whenever you press Save.
If you select "For Transfer to CD/DVD”, the images
are saved to the HDD buffer.
14. Repeat this step for as many images/clips you want
to save.
15. After you have added all of the images/loops you
want to save and are ready to write to the media,
transfer all the images at the same time. Press Menu
-->Save As--> Transfer To CD/DVD.
A progress bar let you know that the “Media transfer
is in progress.”
16. If you do not want to save this image, select “Delete
Files For Transfer.”
17. Press F3 to eject the media. Select CD / DVD
Recordable. Select Yes and Verify Files. This
compares the expected number of files with the
actual number of files on the media. The files are
also checked to ensure that they are readable.
NOTE: The Report Save As feature is somewhat
different. As soon as you select to save a report, the
report is saved.
NOTE: If you save 3D/4D image as AVI. file, an
annotation text “COMP” appears at the top of the saved
image which represent the compressed image.
NOTE: Time line image can be saved as multi frames
image with SaveAs. 3D/4D images can't be saved with
WMV format.
LOGIQ 7/LOGIQ 7 Pro Quick Guide
Connectivity
Connectivity on the LOGIQ 7/LOGIQ 7 Pro is based on
the Dataflow concept.
Login as Administrator. Select Utility. Select
Connectivity. Configure the menus from left to
right, starting with TCP/IP first. When finished
making connectivity changes to the utility menus,
restart the system.
Direction 5307393-100 Rev. 1 24
TCP/IP Services
Type in the Computer’s Name. Identify the Ultrasound To add the services,
system to the rest of the network by filling in its IP
1. Select the destination device.
Address, Subnet Mask, and Gateway (if applicable).
Press Save. 2. Select the service to add and press Add.
3. Type the name in the Name Field.
4. Specify Properties in the Properties boxes (located in
the upper right-hand side and lower left-hand side).
5. Press Save.
There are two service types that pertain to printers:
• Standard Printer is used for digital peripherals.
• Video Capture Device is used for devices that are
triggered by a contact closure, typically analog
devices.

Device
1. Press Add.
2. Type the name of the device and its IP address.
3. Press Save.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 25

Dataflow Buttons Miscellaneous

A dataflow is a set of pre-configured services. For You can assign print buttons to a device or to a dataflow. Set up Patient/Exam menu options and Printer and Store
example, DICOM services may be for storage, worklist, Options
1. Select the print button to configure and the properties
verify, etc. In addition, there are other service types like
on the left of the screen.
video print, standard color print, storage to local hard
drive, select patient from local database, etc. 2. Select the service you want to use and press >> to
add to Printflow view.
Set up dataflows for the services. 3. Select the Standard Print under Active Images Page
1. Press Add and type the dataflow name in the name as necessary.
field. Select the service you want to use and press 4. Press Save.
>> to add to Dataflow view.
NOTE: You can configure each print key to multiple
2. Press Save. output devices/workflow.

Removable Media
Format and verifying media.

Image/ Patient Management

and Connectivity
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 26
DICOM Status
Status Description
To check the status of all DICOM jobs or redirect DICOM
jobs, press F4. FAILED Failed. It stays in spooler. Select Retry or
delete for the job to complete.

DONE Finished successfully

Status Description

HOLD Waiting for a user activity. Select Resend

or Send-To for the job to complete.

Pending Waiting for the previous jobs to finish.

(The previous jobs may be Active or
Pending). It will go directly without user
interaction.

Append Not completed. For example Direct

Storing job waiting for more images, New
Patient or End Current Patient. Or it
could be a print job with 3x3 images,
which only has 8 images and waiting for
1 more image, New Patient or End
Current Patient..

Active Active is actually being sent on the

network (or trying to connect).

SUCCESS Successfully sent.

LOGIQ 7/LOGIQ 7 Pro Quick Guide
Using CINE
Activating CINE
Press Freeze, then roll the Trackball to activate CINE. To
start CINE Loop playback, press Run/Stop. To stop CINE
Loop playback. press Run/Stop.
To activate Timeline CINE, press Freeze, press Scan
Area, then roll the Trackball to activate CINE.
Quickly Move to Start/End Frame
Press First to move to the first CINE frame; press Last to
move to the last CINE frame.
Select all
Press Select All to select all frames of cineloop.
Select numbers of heart cycles
Press left or right arrow to select the number of heart
cycle to review.
Select the heart cycle
Rotate the Cycle select knob clockwise/counterclockwise
to select the heart cycle of interest.
Synchronize the cine loops.
1. Scan and freeze for the first cine loop.
2. Press L or R to display dual display mode.
3. Scan and freeze for the second cine loop.
4. Press Synch mode to start the synchronization.
Direction 5307393-100 Rev. 1
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 clockwise/counter-clockwise to
increase/decrease the CINE Loop playback speed.
Disconnecting B-Mode CINE from Timeline
CINE
To review the B-Mode CINE Loop only, press Cine Mode
Selection and select B Only.
To review the Timeline CINE Loop only, press Cine Mode
Selection and select TL Only.
To return to linked B-Mode and Timeline CINE Loop
review, press Cine Mode Selection and select B/TL.
Moving through a CINE Loop
Frame By Frame
Turn Frame by Frame to move through
CINE memory one frame at a time.
27
Cine Capture
Selecting Cine Capture will search through all images
between the start frame and end frame and display each
peak or the highest velocity/tissue power. Adjust the start
frame and end frame points to limit the image frames
used in the process.
NOTE: Cine Capture is applied only for 2D images (B,
CF, PDI, Contrast, TAD, e.t.c.).
1. Display the cineloop which is on-memory or recalled
from the archive.
2. Run the cineloop.
3. Press Cine Capture on the touch panel to display
captured image.
4. If necessary, save the captured image.
5. Press Cine Capture again to off.
Enhancement. Executes the enhancement
process to the cine capture images.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 28

Easy 3D

Acquiring a 3D Scan Adjusting the 3D Volume of Interest

1. Optimize the B-Mode image. Ensure even gel You can colorize the 3D volume of interest.
coverage.
You can resize the VOI by adjusting the scan distance.
2. Press the 3D control panel key. Two screens appear.
3. To start acquiring the 3D image, press ‘L’ (the left Performing a Surface Render
split screen key).
From the 3D Touch Panel, press 3D, then press Texture
4. To perform a parallel scan, scan evenly. To perform a on the next Touch Panel to add a photorealistic/clay-like
sweep (fan) scan, rock the probe once. Note the quality to the render.
distance of the scan.
5. The 3D volume of interest is generated on the right Adjust the opacity and density via Threshold/Opacity
side of the screen in real time. (press the key to adjust opacity). This adjusts what ‘grays’
the system recognizes, allowing you to emphasize/de-
NOTE: If the image stops before you’re done scanning, emphasize grays as necessary.
start acquiring the 3D volume of interest again.
6. To stop the 3D scan, press ‘R’ (the right split screen Scalpel
key). To cut away portions of the anatomy,

Manipulating the 3D Scan 1. Press Scalpel. A caliper appears on the 3D VOI.

2. Press Set to set the caliper. Trackball around the
Imagine you are able to manipulate the 3D volume of portion to be cut away.
interest (VOI) in your hand.
3. Double click and apply the scalpel.
You can rotate it left to right or right to left. You can rotate 4. Change the projection and scalpel again.
it forward/backward (white hand).
NOTE: You can undo one scalpel, then check apply on
Then, imagine that you can view the volume of interest side of monitor.
one slice at a time through the anatomy (red hand).
Also imagine that you are able to pull back tissue to view 3DView Scanning Hints
specific portions of anatomy (yellow and green hands). Set the appropriate values for the 3D Acq Mode and Scan
The 3D volume of interest is a tangible anatomical object Plane.
that you can see and manipulate easily using the It is advisable to set the scan distance before the scan
Trackball and Set control panel keys. begins.
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.

Post Processing
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 29
Contact Information

INTERNET OTHER COUNTRIES ARGENTINA

http://www.gehealthcare.com/ NO TOLL FREE GEME S.A.
TEL: international code + 33 1 39 20 0007 Miranda 5237
USA Buenos Aires - 1407
CANADA TEL: (1) 639-1619 -- FAX: (1) 567-2678
GE Healthcare GE Medical Systems
Ultrasound Service Engineering AUSTRIA
Ultrasound Svc Engineering TEL: (1) 800-664-0732
9900 Innovation Drive 4855 W. Electric Avenue GE GesmbH Medical Systems Austria
Wauwatosa, WI 53226 Milwaukee, WI 53219 Prinz Eugen Strasse 8/8
TEL: (1) 800-437-1171 or FAX: (1) 414-647-409 Customer Answer Center TEL: (1) 262-524-5698 A-1040 WIEN
TLX: 136314
Clinical Questions LATIN & SOUTH AMERICA TEL: 0660 8459 toll free -- FAX: +43 1 505 38 74
For information in the United States, Canada, GE Medical Systems
Mexico and parts of the Caribbean, call the BELGIUM
Ultrasound Svc Engineering TEL: (1) 262-524-5300
Customer Answer Center: 4855 W. Electric Avenue GE Medical Systems Benelux
TEL: (1) 800-682-5327 or (1) 262-524-5698 Milwaukee, WI 53219 Gulkenrodestraat 3
In other locations, contact your local Applications, Customer Answer Center TEL: (1) 262-524-5698 B-2160 WOMMELGEM
Sales or Service Representative. TEL: 0 800 11733 toll free
EUROPE FAX: +32 0 3 320 12 59
Service Questions
GE Ultraschall TLX: 72722
For service in the United States, call GE CARES Deutschland GmbH & Co. KG
TEL: (1) 800-437-1171 BRAZIL
Beethovenstraße 239
Postfach 11 05 60 GE Sistemas Médicos
Accessories Catalog Requests
D-42655 Solingen -- TEL: 0130 81 6370 toll free Av Nove de Julho 5229
To request the latest GE Accessories catalog or TEL: (49) 212.28.02.207 -- FAX: (49) 212.28.02.431 01407-907 São Paulo SP
equipment brochures in the United States, call the TEL: 0800-122345 -- FAX: (011) 3067-8298
Response Center: TEL: (1) 800-643-6439 ASIA
In other locations, contact your local Applications, CHINA
GE Ultrasound Asia TEL: 65-291-8528
Sales or Service Representative. On-Line Center (OLC), Asia FAX: 65-272-3997 GE Healthcare - Asia TEL: (8610) 5806 9403
No. 1, Yongchang North Road FAX: (8610) 6787
Placing an Order JAPAN 1162
To place an order, order supplies or ask an GE Yokogawa Medical Systems Beijing Economic & Technology Development Area
accessory-related question in the United States, call Customer Call Center TEL: 0120-055-919 toll free Beijing 100176, China
the GE Access Center: TEL: (1) 800-472-3666 FAX: (81) 42-648-2905
In other locations, contact your local Applications,
Sales or Service Representative.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 30

DENMARK LUXEMBOURG SPAIN

GE Medical Systems TEL: 0800 2603 toll free GE Medical Systems España
Fabriksparken 20 Hierro 1 Arturo Gimeno
DK-2600 GLOSTRUP MEXICO Poligono Industrial I
TEL: +45 4348 5400 -- FAX: +45 4348 5399 GE Sistemas Médicos de Mexico S.A. de C.V. E-28850 TORREJON DE ARDOZ
Rio Lerma #302, 1º y 2º Pisos TEL:900 95 3349 free -- FAX: +34 1 675 3364
FRANCE TLX: 22384 A/B GEMDE
Colonia Cuauhtémoc
GE Medical Systems 06500-México, D.F.
SWEDEN
738 rue Yves Carmen TEL: (5) 228-9600 -- FAX: (5) 211-4631
F-92658 BOULOGNE CEDEX GE Medical Systems
TEL: 05 49 33 71 toll free -- FAX: +33 1 46 10 01 20 NETHERLANDS PO-BOX 1243
GE Medical Systems Nederland B.V. S-16428 KISTA
GERMANY TEL: 020 795 433 toll free -- FAX: +46 87 51 30 90
Atoomweg 512
GE Ultraschall NL-3542 AB UTRECHT TLX: 12228 CGRSWES
Deutschland GmbH & Co. KG TEL: 06 022 3797 toll free -- FAX: +31 304 11702
SWITZERLAND
Beethovenstraße 239
Postfach 11 05 60 POLAND GE Medical Systems (Schweiz) AG
D-42655 Solingen GE Medical Systems Polska Sternmattweg 1
TEL: 0130 81 6370 toll free Krzywickiego 34 CH-6010 KRIENS
TEL: (49) 212.28.02.207 -- FAX: (49) 212.28.02.431 P-02-078 WARSZAWA TEL: 155 5306 -- FAX: +41 41 421859
TEL: +48 2 625 59 62 -- FAX: +48 2 615 59 66
GREECE TURKEY
GE Medical Systems Hellas PORTUGAL GE Med. Sys. Turkiye A.S.
41, Nikolaou Plastira Street GE Medical Systems Portuguesa S.A. Mevluk Pehliran Sodak
G-171 21 NEA SMYRNI Rua Sa da Bandeira, 585 Yilmaz Han, No 24 Kat 1
TEL: +30 1 93 24 582 -- FAX: +30 1 93 58 414 Apartado 4094 TLX: 22804 Gayretteppe
P-4002 PORTO CODEX ISTANBUL
ITALY TEL: 05 05 33 7313 toll free - FAX: +351 2 2084494 TEL: +90 212 75 5552 -- FAX: +90 212 211 2571
GE Medical Systems Italia
Via Monte Albenza 9 RUSSIA UNITED KINGDOM
I-20052 MONZA GE VNIIEM GE Medical Systems
TEL: 1678 744 73 toll free -- FAX: +39 39 73 37 86 Mantulinskaya UI. 5A Coolidge House
TLX: 3333 28 123100 MOSCOW 352 Buckingham Avenue
TEL: +7 095 956 7037 -- FAX: +7 502 220 32 59 SLOUGH
TLX: 613020 GEMED SU Berkshire SL1 4ER
TEL: 0800 89 7905 toll free -- FAX: +44 753 696067

Contact Information
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 31
Documentation

Introduction Using Online Help Via F1 Navigating Through Help

Documentation is being provided via:
• Online Help (on the Ultrasound Scanner via F1)
• Basic User Manual
• Advanced Reference Manual
• Quick Guide
• Quick Card(s)
• Release Notes and Workarounds
• Basic Service Manual
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
Online Help is organized like a manual, with
individual chapters, sections, and pages.
Click on the plus (+) sign next to MANUAL to open
up the book.
Click on the plus sign next to the chapter you want
to view to open up that chapter.
Click on the plus sign next to the chapter you want
to view to open up that section.
Click to open up the page to view that page’s
information.
The blue, underlined text links you to related topics.
Click on the link to move to the new topic.
To go back to the previous screen, press Back. To
return to the link, press Forward.
LOGIQ 7/LOGIQ 7 Pro Quick Guide
Help Links
After you click on a blue, underlined portion of text,
the screen updates with this link’s content.
Searching for a Topic in Help
To search for a specific topic, click on the Search
tab. Type in the topic name in the Type in the
keyword to find: field. Topics with the word or
phrase you typed appear in the Select Topic to
display: area. Either double click on the topic you
want to view or highlight the topic and press the
Display button to view this topic.
Direction 5307393-100 Rev. 1
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.
32
Using the Help Index
Or, you can look for topics by using the Index. Press
the Index tab, then use the scroll bar to look up a
topic.
Other Help Features
To hide the left side of the screen, press the Hide
icon at the upper, left-hand portion of the screen. To
view the left side of the screen again, press the
Show icon at the upper, left-hand portion of the
screen.
To size the Help window, position and hold down
the cursor at the corner of the screen while moving
the Trackball.
To move the Help window to the Touch Panel
display, position and hold down the cursor at the
very top of the Help window while moving the
Trackball to the Touch Panel display.
Exiting Online Help
To exit Online Help, press the ‘X’ in the upper, right-
hand corner of the Online Help window.
Electronic Documentation
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 33
Accessing Documentation Via a PC 3. Press Utilities and insert the CD-ROM. 5. Select Scanner Documentation Interface.

To view user documentation on a PC,

1. Insert the CD into the CD drive.
2. Open the CD drive on your desktop.
3. Double click on the ‘gedocumentation.html’
document.
4. Select the item you want to view (click on the
blue, underlined link in the File Name column).
To close the window, click on the ‘X’ in the upper,
right-hand corner of the browser window.
NOTE: If your PC does not have the Adobe
Acrobat Reader, the PC version is supplied on the 4. Select Scanner Utilities.
6. Scroll to find the document, double click on the
CD. Open the CD and double click on document, and open it.
‘ar505enu.exe. Follow the prompts to install Adobe
Acrobat Reader on your PC.

Accessing Documentation on the

Ultrasound Scanner Via the CD-ROM

To access documentation via the CD-ROM,

1. Press Utility. Press Service.
2. Logon as ‘Operator’ next to Select User Level.
Enter the following password: ‘uls’. Press Okay.

NOTE: You can search through a document, use

hyperlinks in the Table of Contents and Index to
locate topics, and navigate via bookmarks.
NOTE: In addition to viewing documentation on the
Ultrasound system, the Documentation CD can be
read on any PC.
To exit, press the ‘X’ in the upper, right-hand corner
of the documentation window.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 34

Precaution Levels

Icon description

Various levels of safety precautions may be found on the equipment and different levels of concern are identified by one of the following flag words and icons which
precede the precautionary statement.

DANGER Indicates that a specific hazard is known to exist which through inappropriate conditions or actions will cause:
• Severe or fatal personal injury
• Substantial property damage.

WARNING Indicates that a specific hazard is known to exist which through inappropriate conditions or actions may cause:
• Severe personal injury
• Substantial property damage.

Indicates that a potential hazard may exist which through inappropriate conditions or actions will or can cause:
CAUTION
• Minor injury
• Property damage.

NOTE: Indicates precautions or recommendations that should be used in the operation of the ultrasound system, specifically:
• Maintaining an optimum system environment
• Using this Manual
• Notes to emphasize or clarify a point.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 35
Hazard Symbols - Icon Description
Potential hazards are indicated by the following icons:

Table 1-1: Potential Hazards

Icon Potential Hazard Usage Source

Biological • Patient/user infection due to contaminated equipment. • Cleaning and care instructions ISO 7000
Hazard • Sheath and glove guidelines No. 0659

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

• ECG
Hazard • Connections to back panel

Moving • Console, accessories or optional storage devices that can fall on patient, user, or others. • Moving
• Collision with persons or objects result in injury while maneuvering or during system • Using brakes
Hazard
transport. • Transporting
• Injury to user from moving the console.

Acoustic • Patient injury or tissue damage from ultrasound radiation. • ALARA, the use of power output following
Output the as low as reasonably achievable
principle
Hazard

Explosion • Risk of explosion if used in the presence of flammable anesthetics. • Flammable anesthetic
Hazard

Smoke & • Patient/user injury or adverse reaction from fire or smoke. • Replacing fuses
Fire Hazard • Patient/use injury from explosion and fire. • Outlet guidelines

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 36

Important Safety Considerations

The following topic headings (Patient Safety, and Equipment and Personnel Safety) are intended to make the equipment user aware of particular hazards
associated with the use of this equipment and the extent to which injury can occur if precautions are not observed. Additional precautions may be provided
throughout the manual.

Improper use can result in serious injury. The user must be thoroughly familiar with the instructions and potential hazards involving ultrasound
CAUTION
examination before attempting to use the device. Training assistance is available from GE Medical Systems if needed.
The equipment user is obligated to be familiar with these concerns and avoid conditions that could result in injury.

Patient Safety

Related Hazards

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

Patient identification

Always include proper identification with all patient data and verify the accuracy of the patient's name or ID numbers when entering such data. Make sure correct
patient ID is provided on all recorded data and hard copy prints. Identification errors could result in an incorrect diagnosis.
Diagnostic information

Equipment malfunction or incorrect settings can result in measurement errors or failure to detect details within the image. The equipment user must become
thoroughly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctions. Applications training is available through
the local GE representative. Added confidence in the equipment operation can be gained by establishing a quality assurance program.

The system’s acoustic output remains transmitting when the user controls are being used. Allowing the system to transmit acoustic output
CAUTION
with the probe not in use (or in its holder) can cause the probe to build up heat. Always turn off acoustic output or freeze the image when not
in use.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 37
Related Hazards (continued)

Mechanical hazards

The use of damaged probes or improper use and manipulation of intracavitary probes can result in injury or increased risk of infection. Inspect probes often for
sharp, pointed, or rough surface damage that could cause injury or tear protective barriers. Never use excessive force when manipulating intracavity probes.
Become familiar with all instructions and precautions provided with special purpose probes.
The use of damaged probes can result in injury or increased risk of infection. Inspect probes often for sharp, pointed, or rough surface damage that could cause
injury or tear protective barriers. Become familiar with all instructions and precautions provided with special purpose probes

Electrical A damaged probe can also increase the risk of electric shock if conductive solutions come in contact with internal live parts. Inspect probes
Hazard often for cracks or openings in the housing and holes in and around the acoustic lens or other damage that could allow liquid entry.
Become familiar with the probe's use and care precautions outlined in Probes and Biopsy.

Ultrasound transducers are sensitive instruments which can easily be damaged by rough handling. Take extra care not to drop
CAUTION
transducers and avoid contact with sharp or abrasive surfaces. A damaged housing, lens or cable can result in patient injury or serious
impairment or operation.

Ultrasound can produce harmful effects in tissue and potentially result in patient injury. Always minimize exposure time and keep
CAUTION
ultrasound levels low when there is no medical benefit. Use the principle of ALARA (As Low As Reasonably Achievable), increasing output
only when needed to obtain diagnostic image quality. Observe the acoustic output display and be familiar with all controls affecting the
output level. See the Bioeffects section of the Acoustic Output chapter in the Advanced Reference Manual for more information.

Do not use with Defibrillator.

CAUTION
This equipment does not have a defibrillator approved applied part.

Training

It is recommended that all users receive proper training in applications before performing them in a clinical setting. Please contact the local GE representative for
training assistance.
ALARA training is provided by GE Application Specialists. The ALARA education program for the clinical end-user covers basic ultrasound principles, possible
biological effects, the derivation and meaning of the indices, ALARA principles, and examples of specific applications of the ALARA principle.

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 38

Equipment and Personnel Safety

Related 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 the proper action for the patient. Inform a
qualified service person and contact a Service Representative for information.
There are no user serviceable components inside the console. Refer all servicing to qualified service personnel only.

WARNING Only approved and recommended peripherals and accessories should be used. All peripherals and accessories must be securely
mounted to the LOGIQ 7/LOGIQ 7 Pro.

DANGER The concerns listed below can seriously affect the safety of equipment and personnel during a diagnostic ultrasound examination.

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

Hazard

This equipment provides no special means of protection from high frequency (HF) burns that may result from using an electrosurgical unit
CAUTION
(ESU). To reduce the risk of HF burns, avoid contact between the patient and ultrasound transducer while operating the ESU. Where
contact cannot be avoided, as in the case of TEE monitoring during surgery, make sure the transducer is not located between the ESU
active and dispersive electrodes and keep the ESU cables away from the transducer cable.

Electrical To avoid injury:

Hazard • Do not remove protective covers. No user serviceable parts are inside. Refer servicing to qualified service personnel.
• To assure adequate grounding, connect the attachment plug to a reliable (hospital grade) grounding outlet.
• Never use any adaptor or converter of a three-prong-to-two-prong type to connect with a mains power plug. The protective earth
connection will loosen.
• Do not place liquids on or above the console. Spilled liquid may contact live parts and increase the risk of shock.
• Plug any peripherals into the LOGIQ 7/LOGIQ 7 Pro AC power outlet.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 39
Related Hazards (continued)

Do not use this equipment if a safety problem is known to exist. Have the unit repaired and performance verified by qualified service
CAUTION
personnel before returning to use.

Smoke & The system must be supplied from an adequately rated electrical circuit. The capacity of the supply circuit must be as specified in
Fire Hazard Chapter 3 of the Basic User Manual.

Biological For patient and personnel safety, be aware of biological hazards while performing invasive procedures. To avoid the risk of disease
Hazard transmission:
• Use protective barriers (gloves and probe sheaths) whenever possible. Follow sterile procedures when appropriate.
• Thoroughly clean probes and reusable accessories after each patient examination and disinfect or sterilize as needed. Refer to
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 they apply to personnel and equipment.

Contact with natural rubber latex may cause a severe anaphylactic reaction in persons sensitive to the natural latex protein. Sensitive
CAUTION
users and patients must avoid contact with these items. Refer to package labeling to determine latex content and FDA’s March 29, 1991
Medical Alert on latex products.

The system is equipped with an Auto Freeze feature which disables acoustic output and freezes the image when the system is not in use.
CAUTION
Take care when deactivating this feature.

When you move the Control Panel up/down with the monitor, place BOTH hands on the Control Panel. Touching other moving parts other
CAUTION
than the Control Panel may cause personal injury.

Never put any device onto the monitor.

CAUTION

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 40

Related Hazards (continued)

Archived data is managed at the individual sites. Performing data backup (to any device) is recommended on a daily basis.
CAUTION

Do not unpack the LOGIQ 7/LOGIQ 7 Pro. This must be performed by qualified service personnel only.
CAUTION

Do not use the LOGIQ 7/LOGIQ 7 Pro Ultrasound system ECG wave for diagnosis and monitoring.
CAUTION

To avoid skin burns in surgical use, do not place ECG electrodes in current path between Electrosurgical Unit (ESU) active and dispersive
CAUTION
electrodes. Keep ESU cables away from ECG leads.
.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 41
Device Labels

Label Icon Description

The following table describes the purpose and location of safety labels and other important information provided on the equipment.

Table 1-2: Label Icons

Label/Icon Purpose/Meaning Location

Identification and Rating Plate Manufacture’s name and address See “Warning Label and Caution Label
Date of manufacture Locations” on page 55.
Model and serial numbers
Electrical ratings (Volts, Amps, phase, and frequency)

Type/Class Label Used to indicate the degree of safety or protection.

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

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

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

“ATTENTION” - Consult accompanying documents” is intended to alert the user to refer to the operator manual Various
or other instructions when complete information cannot be provided on the label.
!
“General Warning Sign” Rear panel and UPS battery

“Warning” - Dangerous voltage” (the lightning flash with arrowhead) is used to indicate electric shock hazards. Rear panel and inside of console

“Mains OFF” indicates the power off position of the mains power breaker. Refer to Chapter 3 in the Basic User Manual for
location information.

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 42

Table 1-2: Label Icons

Label/Icon Purpose/Meaning Location

“Mains ON” indicates the power on position of the mains power breaker. Refer to Chapter 3 in the Basic User Manual for
location information.

“ON” indicates the power on position of the power switch. See “Power Switch Location” on page 1.
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. Rear panel

““Equipotentiality” indicates the terminal to be used for connecting equipotential conductors when Rear panel
interconnecting (grounding) with other equipment.
Connection of additional protective earth conductors or potential equalization conductors is not necessary in
most cases and is only recommended for situations involving multiple equipment in a high-risk patient
environment to provide assurance that all equipment is at the same potential and operates within acceptable
leakage current limits. An example of a high-risk patient would be a special procedure where the patient has
an accessible conductive path to the heart such as exposed cardiac pacing leads.

Alternating Current symbol is in accordance with IEC 60878-01-14. Rear Panel, Circuit breaker label of console and
front panel (if applicable).
Rating plate

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

No hazardous substance, above the maximum concentration value, is present. Maximum concentration values
for electronic information products, as set by the People’s Republic of China Electronic Industry Standard SJ/
T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium,
polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE).

Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum Probe
concentration values for electronic information products, as set by the People’s Republic of China Electronic
Industry Standard SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium,
cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE). “10” indicates the
number of years during which the hazardous substance(s) will not leak or mutate so that the use of this product
will not result in any severe environmental pollution, bodily injury, or damage to any assets.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 43
Table 1-2: Label Icons

Label/Icon Purpose/Meaning Location

Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum Rear Panel
concentration values for electronic information products, as set by the People’s Republic of China Electronic
Industry Standard SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium,
cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE). “20” indicates the
number of years during which the hazardous substance(s) will not leak or mutate so that the use of this product
will not result in any severe environmental pollution, bodily injury, or damage to any assets.

Do not use the following devices near this equipment: cellular phone, radio receiver, mobile radio transmitter, Rear
radio controlled toy, etc. Use of these devices near this equipment could cause this equipment to perform
outside the published specifications. Keep power to these devices turned off when near this equipment.

Do not place a finger, hand or any object on the joint of the monitor or monitor arm to avoid injury when moving Rear of the LCD monitor
the monitor and monitor arm.

Pay attention to the monitor arm position to avoid hitting it against anyone or anything. Monitor arm
CAUTION

This product consists of devices that may contain mercury, which must be recycled or disposed of in Rear of console
accordance with local, state, or country laws. (Within this system, the backlight lamps in the monitor display,
contain mercury.)

The GOST Mark indicates this equipment conforms with the Federal Agency on Technical Regulating and Rating plate of 220V system
Metrology of Russia

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 44

Classifications
Type of protection against electric shock
Class I Equipment (*1)
Degree of protection against electric shock
Type BF Applied part (*2) (for PCG, Probes marked with BF symbol)
Type CF Applied part (*3) (for ECG, Probes marked with CF symbol)
Continuous Operation
System is Ordinary Equipment (IPX0)
Footswitch is IPX8

*1. Class I EQUIPMENT

EQUIPMENT in which protection against electric shock does not rely on BASIC INSULATION only, but includes an earth ground. This additional safety precaution
prevents exposed metal parts from becoming LIVE in the event of an insulation failure.

*2. Type BF APPLIED PART

TYPE BF APPLIED PART providing a specified degree of protection against electric shock, with particular regard to allowable LEAKAGE CURRENT.

Table 1-3: Type BF Equipment

Normal Mode Single fault condition

Patient leakage current Less than 100 microA Less than 500 microA

*3. Type CF APPLIED PART

Type CF Applied Part providing a degree of protection higher than that for TYPE BF Applied Part against electric shock particularly regarding allowable LEAKAGE
CURRENTS.

Table 1-4: Type CF Equipment

Normal Mode Single fault condition

Patient leakage current Less than 10 microA Less than 50 microA

LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 45
EMC (Electromagnetic Compatibility)
NOTE: This equipment generates, uses and can radiate radio frequency energy. The equipment may cause radio frequency interference to other medical and non-
medical devices and radio communications. To provide reasonable protection against such interference, this product complies with emissions limits for a Group 1,
Class A as stated in IEC/EN 60601-1-2:2001. However, there is no guarantee that interference will not occur in a particular installation.
NOTE: If this equipment is found to cause interference (which may be determined by turning the equipment on and off), the user (or qualified service personnel)
should attempt to correct the problem by one or more of the following measure(s):
• reorient or relocate the affected device(s)
• increase the separation between the equipment and the affected device
• power the equipment from a source different from that of the affected device
• consult the point of purchase or service representative for further suggestions.
NOTE: The manufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or
modifications to this equipment. Unauthorized changes or modifications could void the users’ authority to operate the equipment.
NOTE: To comply with the regulations on electromagnetic interference for a Group1/Class A, all interconnect cables to peripheral devices must be shielded and
properly grounded. Use of cables not properly shielded and grounded may result in the equipment causing radio frequency interference in violation of the
regulations.
NOTE: Do not use devices which intentionally transmit RF Signals (cellular phones, transceivers, or radio controlled products) other than those supplied by GE
(wireless microphone, for example) in the vicinity of the equipment as it may cause performance outside the published specifications. Keep the power to these type
devices turned off when near this equipment.
The medical staff in charge of this equipment is required to instruct technicians, patients, and other people who maybe around this equipment to fully comply with the
above requirement.

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 46

EMC (Electromagnetic Compatibility) (continued)

EMC Performance

All types of electronic equipment may characteristically cause electromagnetic interference with other equipment, either transmitted through air or connecting
cables. The term EMC (Electromagnetic Compatibility) indicates the capability of equipment to curb electromagnetic influence from other equipment and at the same
time not affect other equipment with similar electromagnetic radiation from itself.
Proper installation following the service manual is required in order to achieve the full EMC performance of the product.
The product must be installed as stipulated in 4.2, Notice upon Installation of Product.
In case of issues related to EMC, please call your service personnel.
The manufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or modifications
to this equipment. Unauthorized changes or modifications could void the users’ authority to operate the equipment.

Do not use devices which intentionally transmit RF signals (cellular phones, transceivers, or radio controlled products), other than those
CAUTION
supplied by GE (wireless microphone, for example) unless intended for use with this system, in the vicinity of this equipment as it may
cause performance outside the published specifications.
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 people who may be around this equipment
to fully comply with the above regulation.

Portable and mobile radio communications equipment (e.g. two-way radio, cellular/cordless telephones, wireless computer networks) other than those supplied by
GE (wireless microphone, for example) should be used no closer to any part of this system, including cables, than determined according to the following method:
Table 1-5: Portable and mobile radio communications equipment distance requirements

Frequency Range: 150 kHz - 80 MHz 80 MHz - 800 MHz 800 MHz - 2.5 GHz

Calculation Method: d=[3.5/V1] square root of P d = [3.5/E1] square root of P d = [7/E1] square root of P

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

If the maximum transmitter power in

watts is rated The separation distance in meters should be

5 2.6 2.6 5.2

20 5.2 5.2 10.5

100 12.0 12.0 24.0

LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 47
Notice upon Installation of Product

Separation distance and effect from fixed radio communications equipment: field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast transmitter cannot be predicted theoretically with accuracy. To
assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the
location in which the ultrasound system is used exceeds the applicable RF compliance level as stated in the immunity declaration, the ultrasound system should be
observed to verify normal operation. If abnormal operation is observed, additional measures may be necessary, such as re-orienting or relocating the ultrasound
system or using an RF shielded examination room may be necessary.
1. Use either power supply cords provided by GE Medical Systems or ones designated by GE Medical Systems. Products equipped with a power source plug
should be plugged into the fixed power socket which has the protective grounding conductor. Never use any adaptor or converter to connect with a power
source plug (i.e. three-prong-to-two-prong converter).
2. Locate the equipment as far away as possible from other electronic equipment.
3. Be sure to use only the cables provided by or designated by GE Medical Systems. Connect these cables following the installation procedures (i.e. wire power
cables separately from signal cables).
4. Lay out the main equipment and other peripherals following the installation procedures described in the Option Installation manuals.

General Notice

1. Designation of Peripheral Equipment Connectable to This Product.

The equipment indicated on Chapter 15 of the Basic User Manual can be hooked up to the product without compromising its EMC performance.
Avoid using equipment not designated in the list. Failure to comply with this instruction may result in poor EMC performance of the product.
2. Notice against User Modification
The user should never modify this product. User modifications may cause degradation in EMC performance.
Modification of the product includes changes in:
a. Cables (length, material, wiring, etc.)
b. System installation/layout
c. System configuration/components
d. Securing system parts (cover open/close, cover screwing)
3. Operate the system with all covers closed. If a cover is opened for some reason, be sure to shut it before starting/resuming operation.
4. Operating the system with any cover open may affect EMC performance.

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 48

Peripheral Update for EC countries

The following is intended to provide the users in EC countries with updated information concerning the connection of the LOGIQ 7/LOGIQ 7 Pro to image recording
and other devices or communication networks.
The LOGIQ 7/LOGIQ 7 Pro has been verified for overall safety, compatibility and compliance with the following on-board image recording devices:
• Sony UP-895 MDW/D895MD Digital Printer
• Sony UP-D21MD Color Printer
• Sony UP-D23MD Color Printer
• Sony UP-D55 Color Printer
• Sony UP-51MD Color Printer
• Sony SVO9500MD2/MD2P Video Cassette Recorder
• Mitsubishi 91DW B&W Printer
• Mitsubishi P93W B&W Printer
• Mitsubishi CP900/800 Color Printer
• Mitsubishi CP30DW Color Printer
• Mitsubishi VCR HV-MD3000/HS-MD3000U/HS-MD3000E
• Wired/Wireless Microphone
• Panasonic LQ-MD800/800P/800E DVD Recorder
The LOGIQ 7/LOGIQ 7 Pro has also been verified for compatibility, and compliance for connection to a local area network (LAN) via the rear panel Ethernet
connection, provided the LAN components are IEC/EN 60950 compliant.
Connection may also be made to a CE Marked and IEC/EN 60950 compliant modem using one of the serial ports at the rear panel.
The LOGIQ 7/LOGIQ 7 Pro may also be used safely while connected to devices other than those recommended above if the devices and their specifications,
installation, and interconnection with the system conform to the requirements of IEC/EN 60601-1-1.
General precautions for installing an alternate on-board device would include:
1. The added device must have appropriate safety standard conformance and CE Marking.
2. The total power consumption of the added devices, which connect to the LOGIQ 7/LOGIQ 7 Pro and are used simultaneously, must be less than or equal to the
rated supply of the LOGIQ 7/LOGIQ 7 Pro.
3. There must be adequate heat dissipation and ventilation to prevent overheating of the device.
4. There must be adequate mechanical mounting of the device and stability of the combination.
5. Risk and leakage current of the combination must comply with IEC/EN 60601-1.
6. Electromagnetic emissions and immunity of the combination must conform to IEC/EN 60601-1-2.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 49
Peripheral Update for EC countries (continued)

General precautions for installing an alternate off-board, remote device or a network would include:
1. The added device(s) must have appropriate safety standard conformance and CE Marking.
2. The added device(s) must be used for their intended purpose having a compatible interface.
3. Signal or mains isolation devices and additional protective earth may be needed to assure compliance with IEC/EN 60601-1-1.

The connection of equipment or transmission networks other than as specified in the user instructions can result in an electric shock
CAUTION
hazard or equipment malfunction. Substitute or alternate equipment and connections requires verification of compatibility and conformity to
IEC/EN 60601-1-1 by the installer. Equipment modifications and possible resulting malfunctions and electromagnetic interference are the
responsibility of the owner.

Declaration of Emissions

This system is suitable for use in the following environment. The user must assure that it is used only in the electromagnetic environment as specified.

Table 1-6: Declaration of Emissions

Guidance and manufacturer’s declaration - electromagnetic emissions

The system is intended for use in the electromagnetic environment specified below. The user of the system should assure that it is used in such an environment.

Emission Type Compliance Electromagnetic Environment

RF Emissions Group 1 This system uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby
CISPR 11 electronic equipment.

RF Emissions Class A This system is suitable for use in all establishments, other than domestic establishments and those directly connected to the public low-voltage power supply
CISPR 11 network that supplies buildings used for domestic purposes, provided the following warning is heeded:
Warning: This system is intended for use by healthcare professionals only. This system may cause radio interference or may disrupt the operation of nearby
Harmonic Class A
equipment. It may be necessary to take mitigation measures, such as re-orienting or relocating the system or shielding the location.
Emissions
IEC 61000-3-2

Voltage Complies
Fluctuations/Flicker
Emissions
IEC 61000-3-3

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 50

Declaration of Immunity

This system is suitable for use in the following environment. The user must assure that the system is used according to the specified guidance and only in the
electromagnetic environment listed.

Table 1-7: Declaration of Immunity

Immunity Type Test Level Compliance EMC Environment and Guidance

IEC 61000-4-2 ± 6 kV contact ± 6 kV contact Floors should be wood, concrete, or ceramic tile. If floors are
Static discharge covered with synthetic material, the relative humidity should
(ESD) ± 8 kV air ± 8 kV air be at least 30%.
Mains power quality should be that of a typical commercial
IEC 61000-4-4 ± 1 kV for mains ± 1 kV for mains and/or hospital environment. If the user requires continued
Electrical fast operation during power mains interruptions, it is
transient/burst ± 0.5 kV for ECG cable ± 0.5 kV for SIP/SOP recommended that the system be powered from an
uninterruptable power source (UPS) or a battery.
IEC 61000-4-5 Surge Immunity ± 1 kV differential ± 1 kV differential NOTE: UT is the a.c. mains voltage prior to application of the
test level.
± 2 kV common ± 2 kV common
Power frequency magnetic fields should be at levels
characteristic of a typical location in a typical commercial and/
IEC 61000-4-11 < 50T (> 95% dip) for 0.5 cycle; < 50T (> 95% dip) for 0.5 cycle;
or hospital environment.
Voltage dips, short interruptions and 400T (60 0ip) for 5 cycles; 400T (60 0ip) for 5 cycles;
voltage variations on mains supply Separation distance to radio communication equipment must
700T (30 0ip) for 25 cycles; 700T (30 0ip) for 25 cycles; be maintained according to the Table 1-5 on page 46.
< 50T (>95% dip) for 5 sec < 50T (>95% dip) for 5 sec Interference may occur in the vicinity of equipment marked
with the symbol
IEC 61000-4-8 3 A/m 3 A/m
Power frequency (50/60 Hz) magnetic
field

IEC 61000-4-6 3 VRMS 3 VRMS

Conducted RF 150 kHz - 80 MHz 150 kHz - 80 MHz

IEC 61000-4-3 3 V/m 3 V/m

Radiated RF 80 MHz - 2.5 GHz 80 MHz - 2.5 GHz

NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. If noise generated from other electronic
equipment is near the probe’s center frequency, noise may appear on the image. Good power line isolation is required.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 51
Patient Environmental Devices

16 10
17 11
1
18 12 2
14 25
13 21
20 19 3 6
5 9
4 7
15
22 8
23
24

Figure 1. Patient Environmental Devices

1. Peripheral Device (Signals I/O Port, Power In) 11. Signals I/O Port 20. Power Telephone Line
2. Front Panel (Signal I/O Port, Power Out) 12. Power Out 21. Footswitch
3. Non-Imaging Probes 13. Signals I/O Port 22. Power Line (AC~)
4. Imaging Probes 14. Footswitch Connector 23. Ground Line
5. Probe Port 15. Power In 24. Power Cable with Protective Earth
6. 4D probe cable connector 16. Peripheral Devices 25. DVD Multi Drive
7. ECG Cable 17. Signals I/O Port
8. PCG Sensor 18. Power In
9. Physio-Signal Input Panel 19. InSite Modem (Signal I/O Port)
10. Rear Panel

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 52

Acceptable Devices

The devices shown in “Patient Environmental Devices” on page 1-51 are specified to be suitable for use within the PATIENT ENVIRONMENT.

DO NOT connect any probes or accessories without approval by GE within the PATIENT ENVIRONMENT.
CAUTION
See “Peripheral Update for EC countries” on page 48.

Unapproved Devices

Unapproved devices shall not be used in the patient environment.

CAUTION
If devices are connected without the approval of GE, the warranty will be INVALID.
Any device connected to the LOGIQ 7/LOGIQ 7 Pro must conform to one or more of the requirements listed below:
1. IEC standard or equivalent standards appropriate to devices.
2. The devices shall be connected to PROTECTIVE EARTH (GROUND).

Accessories, Options, Supplies

Unsafe operation or malfunction may result. Use only the accessories, options and supplies approved or recommended in these
CAUTION
instructions for use.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 53
Acoustic Output
Located on the upper right section of the system display monitor, the acoustic output display provides the operator with real-time indication of acoustic levels being
generated by the system. See the Acoustic Output chapter in the Advanced Reference Manual for more information. This display is based on NEMA/AIUM
Standards for Real-time Display of Thermal and Mechanic Acoustic Output Indices on Diagnostic Ultrasound Equipment.

Acoustic Output Display Specifications

The display consists of three parts: Thermal Index (TI), Mechanical Index (MI), and a relative Acoustic Output (AO) value. Although not part of the NEMA/AIUM
standard, the AO value informs the user of where the system is operating within the range of available output. Depending on the examination and type of tissue
involved, the TI parameter will be one of three types:
The TI and MI are displayed at all times. The TI display starts at a value of 0.0 and increments in steps of 0.1 The MI display values between 0 and 0.4 increment in
steps of 0.01 and for values greater than 0.4, increments in steps of 0.1.

Thermal Index

Depending on the examination and type of tissue involved, the TI parameter will be one of three types:
• Soft Tissue Thermal Index (TIS). Used when imaging soft tissue only, it provides an estimate of potential temperature increase in soft tissue.
• Bone Thermal Index (TIB). Used when bone is near the focus of the image as in the third trimester OB examination, it provides an estimate of potential
temperature increase in the bone or adjacent soft tissue.
• Cranial Bone Thermal Index (TIC). Used when bone is near the skin surface as in transcranial examination, it provides an estimate of potential temperature
increase in the bone or adjacent soft tissue.
Changing the Thermal Index Type: You can select the displayed TI type on Utility -> Imaging -> B-Mode. This preset is application dependent so each application
could specify a different TI type.

Mechanical Index

Recognizes the importance of non-thermal processes, cavitation in particular, and the Index is an attempt to indicate the probability that they might occur within the
tissue.

Display precision is ±0.1 and accuracy is ±50%. Accuracy of the power output displayed value on the Touch Panel is ±10%.

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 54

Controls Affecting Output

The potential for producing mechanical bioeffects (MI) or thermal bioeffects (TI) can be influenced by certain controls.
The Acoustic Output control has the most significant effect on Acoustic Output.
Indirect effects may occur when adjusting other controls. Controls that can influence MI and TI are detailed under the Bioeffects portion of each control in the Ch 5 of
the Basic User Manual.
Always observe the acoustic output display for possible effects.

Best practices while scanning

HINTS Raise the Acoustic Output only after attempting image optimization with controls that have no effect on Acoustic Output, such as Gain and
TGC.

NOTE: Refer to the Optimization sections of the Basic User Manual Chapter 5 for a complete discussion of each control.

WARNING Be sure to have read and understood control explanations for each Mode used before attempting to adjust the Acoustic Output control or
any control that can effect Acoustic Output.

Acoustic Use the minimum necessary acoustic output to get the best diagnostic image or measurement during an examination. Begin the exam with
Output the probe that provides an optimum focal depth and penetration.
Hazard

Acoustic Output Default Levels

In order to assure that an exam may not start at a high output level, the LOGIQ 7/LOGIQ 7 Pro may initiate scanning at a reduced default output level. This reduced
level is preset programmable and depends upon the exam category and probe selected. It takes effect when the system is powered on or New Patient is selected.
If you want to adjust the acoustic output level manually, turn the dial below Power Output level indicator of the Touch Panel right/left to increase/decrease the level.
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 55
Warning Label and Caution Label Locations

(1)
(1)
(2) (3)
(21) (2) (3)
(4)

(5)
(6) (5)
(17) (6)
(7)
(7)
(10)
(9)
100-120V∼ Label for China
(8)
Japan/USA/Asia Console(100V)

220-240V∼
CAUTION

(18) (11)
제품명 : 초음파영상진단장치
형 명 : LOGIQ 7
수입자 상호 및 주소 : 지이헬스케어코리아 주식회사 (13) (12)
(서 울시 강 남구 청담동 71- 3 지이타 워 7,8,9,10층 ) ETL LISTED
제조회사명, 주소 (제조국) : GE Yokogawa Medical Systems, Ltd (일본) CONFORMS TO
(7- 127, Asahigaoka 4- chome, Hino- shi, Tokyo 191- 8503) UL STD. 2601-1
LISTED R

품목허가번호 : 제 수허 01-1201호 46477

CERTIFIED TO
사용목적 : 환부 에 초 음파 에 너지를 전송, 반사 신호를 수신 하여 생 리학적 CAN/CSA C22.2 NO. 601.1
또는 인공 구 조를 눈으로 볼 수 있도록 하는 기구
제조번호 :
제조년월: YYYY / MM
중 량 : CRT226kg, LCD 212 kg 포 장 단 위 : 1 Set (22) (16)
사용방법 : 사용설명서 참조 사용상 주의사항: 사용 설명서 참조
정격전압 : 220/240 VAC 사용주파수 : 50/60 Hz 通用电气横河医疗系统有限公司
소비전력 : 1200VA
보호형식 : 1급기기 보호정도 : BF형기기 ４－７－１２７，Ａｓａｈｉｇａｏｋａ，Ｈｉｎｏ－ｓｈｉ，Ｔｏｋｙｏ
본 제품은 의료기기임 １９１－８５０３
日本
产品名称：超声诊断扫描仪
型号：ＬＯＧＩＱ ７
ＳＦＤＡ注册号： ＳＦＤＡ （Ｉ） ２００７３２３０５１５
产品标准编号：ＹＺＢ／ＪＡＰ０００４－２００５
产品标准编号：ＹＺＢ／ＪＡＰ －２００６
生产日期：
(14) (15) 输入电压：２２０－２４０Ｖ ￣
输入频率： ５０／６０Ｈｚ
販売名 ：汎用超音波画像診断装置 最大功率： １．２ＫＶＡ
系列号：
定格電源：単相 100V∼
, 05/60Hz
電源入力：1200V
A
型名 ：
製造番号： CAUTION
製造年月：
~ 管理医療機器／特定保守管理医療機器

GE Yokogawa Medical Systems

Figure 2. Warning/Caution label location

Safety
LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 56

Table 1-8: Label Location Explanations

1. Possible shock hazard. Do not remove covers or panels. No user serviceable parts are inside. Refer servicing to qualified service personnel.
2. Do not use the following devices near this equipment: cellular phone, radio receiver, mobile radio transmitter, radio controlled toy, etc. Use of these devices near this equipment could cause this
equipment to perform outside the published specifications. Keep power to these devices turned off when near this equipment.
3. The equipment weighs approximately 225 kg (496 lbs). To avoid possible injury and equipment damage when transporting from one area of use to another:
- Be sure the pathway is clear
- Limit movement to a slow careful walk.
- Use two or more persons to move the equipment on inclines or long distance.
4. Prescription Device (For U.S.A. Only)
5. The CE Mark of Conformity indicates this equipment conforms with the Council Directive 93/42/EEC.
6. WEEE symbol
7. CISPR
CAUTION: The LOGIQ 7/LOGIQ 7 Pro conforms to the CISPR11, Group 1, Class A of the international standard for Electromagnetic disturbance characteristics.
8. Voltage Range (Indication label)
9. Signal ground point label
CAUTION: This is only for “FUNCTIONAL GROUNDING”, NOT “PROTECTIVE EARTH”.
10. Power (Indication label)
11. Grounding reliability can only be achieved when this equipment is connected to a receptacle marked “Hospital Only” or “Hospital Grade”.(For U.S.A., Canada, Japan)
12. ETL Label: NRTL Listing and Certification Mark is used to designate conformance to nationally recognized product safety standards. The Mark bears the name and/or logo of the testing laboratory,
product category, safety standard to which conformity is assessed, and a control number.
13. Identification and Rating Plate–USA/Asia 120V Console
14. Identification and Rating Plate–Europe/Asia/USA 220V Console
15. Identification and Rating Plate–Japan 100V Console
16. Identification and Rating Plate–China Console
17. RoHS Label-China systems only
18. Identification and Rating Plate– Korea
19. Caution label on the monitor
20. Caution label for the range of motion
21. This machine should be used in compliance with law. Some jurisdictions restrict certain uses, such as gender determination. - Korea Console
22. Vermont HG label–USA system only
23. GOST Mark - 220V system only