GE Medical Systems
TechnicalPublications
Direction 2291859-100Rev. 1
LOGIQ 7
Quick Guid
Copyright© 2002 By G
Operating Documenta
0459
e
eneral Electric Co.
tion
GE Medical Systems
GE Medical System: Telex 3797371P. O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.(Asia, Pacific, Latin America, North America)GE Ultraschall TEL: 0130 81 6370 toll freeDeutschland GmbH & Co. KG TEL: (49)(0) 212.28.02.207Beethovenstraße 239, Postfach 11 05 60, D-42655 SolingenGERMANY
Regulatory Requirement
LOGI A
REV0
1
N FOR CHANGEease
lease
aintained on GPC (GE Medical Sales Representative or in the
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Revision History
DATENovember 1, 2001
November 15, 2002
REASOInitial Rel
R2.1.0 Re
List of Effective Page
PAGE REVISIONNUMBER HISTORY
Title Rev. 1A and B Rev. 1
1-54 Rev. 1
Please verify that you are using the latest revision of this document. Information pertaining to this document is mSystems Global Product Configuration). If you need to know the latest revision, contact your distributor, local GEUSA call the GE Ultrasound Clinical Answer Center at 1-800-682-5327 or 262-524-5698.
LOGI B
e United States.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
CAUTION FOR USA ONLY
“United Sates law restricts this device to sale or use by or on the order of a physician” if sold in th
LOGI 1
Pre
Syste
Powe
To con
1. Entyp
2. En
Power switch to turn the power on. The aker must also be in the on position.
igure 1-3. Power Switch Location
. Power Switch Location
a
a
Q 7 Quick Guide Direction 2291859-100 Rev. 1
paring for an Exam
m Power
r On
nect the system to the electrical supply:
sure that the wall outlet is of the appropriate e.
Figure 1-1. Example Plug and Outlet Configurations
1. 100-120 VAC, 1200 VAa, b Plug and Outlet Configuration
2. 220-240 VAC, 1200 VAa, b Plug and Outlet Configuration
sure that the power switch is turned off.
3. Unwrap the power cable. Make sure to allow sufficient slack in the cable so that the plug is not pulled out of the wall if the system is moved slightly.
4. Attach the power plug to the system and secure it in place by using the retaining clamp.
Figure 1-2. Power Plug
a. Retaining clamp for power plug
CAUTION: Ensure that the retaining clamp for the power plug is fixed firmly.
Use caution to ensure that the power cable does not disconnect during system use. If the system is accidentally unplugged, data may be lost.
Press thecircuit bre
F
a
1 2
b a b
a
LOGI 2
Powe
To pow
1. Prsy
2. Th
3. UsShTh(thwh(th
4. DisCleStoda
Q 7 Quick Guide Direction 2291859-100 Rev. 1
r Off
er down the system:
ess the Power switch at the front of the stem once.e System-Exit window is displayed.
ing the Trackball or Tab key, select utdown.e shutdown process takes about 30 seconds e Power On light is green) and is completed en the control panel illumination is turned off e Power On light is amber).connect the probes.an or disinfect all probes as necessary. re them in their shipping cases to avoid
mage.
Starting an Exam
You need to select a pre-configured dataflow that sets up the ultrasound system to work according to the services associated to the dataflow.
1. Select your Operator Login and type in your Password:
2. Press Log on. 3. Fill in the New Patient menu as described on
Page 3.
OR,If the patient name is on the patient record list,
1. Trackball to the patient’s name to highlight the name, (or perform a search to locate the patient) then press Select Patient.
LOGI 3
Pre
Starti
New P
To star
1. Prthe
2. Se3. Ty
etc4. Pr
(Dau
5. Prpro
Selection Window [2]
appropriate exam application.
Selection Window [3]
nt is used to clear the patient entry input a new patient’s data into the . New Exam is used to create a new exam nt patient. Register is used to enter new
formation into the database prior to the m being performed. Exit returns you to
[4]
is exam’s dataflow preference.
formation and Detail Windows [5]
, Name, Birthdate, Age, Sex, Patient’s Telephone Number and Comments
ormation and Detail Windows [6]
pertinent exam specific information.
ist Window [7]
atients in the database. “Search key” earching list by Patient ID, Last Name, e, Birthdate, Sex and Last Exam date. tring” and “Search from” fields help define h parameters. More gives you options like ages and DICOM properties. Delete is ove the selected patient from the
. 3
2
1
4
Q 7 Quick Guide Direction 2291859-100 Rev. 1
paring for an Exam
ng an Exam
atient
t a new patient’s exam,
ess Patient. Press the New Patient button on Patient menu. lect the Exam Category. pe the Patient ID, Patient Name, Birthdate, .
ess the Register button on the Patient menu O NOT press Register if you are tomatically generating a patient ID). ess Scan, B-Mode, Esc, or Exit. Select the be from the Touch Panel.
Probe Selection
Select a probe from the Touch Panel (the system automatically selects the last-used application for this probe).
Patient Entry Menu
Image Management Window [1]
Access to this patient’s exam history and image management features.
Category
Select the
Function
New Patiescreen todatabaseon a currepatient inactual exascanning.
Dataflow
Selects th
Patient In
Patient IDAddress,
Exam Inf
Contains
Patient L
Lists the penables sFirst Nam“Search sthe searcmoving imuse to remdatabase
2
5
7
3
6
1
1
1
1
1
3
2
1
4
5
6
7
LOGI 4
LOGI
1. Toco
AtcofunupbuFoad
2. To3. Vid
ing/Measurement Keys: Clear, Comment, Pattern, Ellipse, Measure, Zoom, M/D r, Scan Area, Set. Press or rotate these
as necessary. . Rotate to adjust the Depth.
ing Feature Keys: Auto Optimize On/Off, B e, Multi Image Left/Right Select. Press keys to activate/deactivate these ons. e and Print Keys. Press Freeze to
e the image; press the P keys to archive, or send the image. Holder. older.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Q 7 Control Panel Tour
uch Panel. Touch the Touch Panel to adjust ntrols.
the bottom of the Touch Panel, there are five mbination rotary dials/push buttons. The ctionality of these keys changes, depending
on the currently displayed menu. Press the tton to switch between controls (as with cus Position/Number), or rotate the dial to just the value.uch Panel Brightness. Rotate to adjust. eo. Press to control the VCR.
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. 7. Additional Feature Keys. Patient, LOGIQView,
3D, Contrast, Harmonics. Press to activate these controls.
8. Keyboard. Use the keyboard to enter patient information and annotations.
9. Mode/Gain Keys: M Mode, Pulsed Wave Doppler (PW) Modes, Power Doppler Imaging (PDI) Mode, Color Flow (CF) Mode, B Mode, and B Flow. Press these key to activate the mode; rotate the key to adjust the Gain.
10. ImagBodyCursokeys,
11. Depth12. Imag
Pausthesefuncti
13. Freezfreezprint,
14. Probe15. Gel H
2
14
4
8
3
15
1 5
147
10 9 12
13
11
6
15
LOGI 5
LOGI
In genthe kekeys:
1. Pr2. Pr
impro
to move to the next Touch Panel page.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Control Panel/Touch Panel Tour
Q 7 Touch Panel Tour
eral, the key status is indicated at the top of y. There are different types of Touch Panel
ess to toggle control on/off.ogression keys are used to assess the pact of the control on the image gressively.
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.
5. Press knob below the Touch Panel to select additional control, then rotate the knob to set values.
6. Press
1
2
6
3
4
5
4
LOGI 6
LOGI
1. InsIde
2. Pa3. Ac4. GE
sy5. Im6. Gr7. Ci
fra
Scale.e Management Menu: Menu, Delete, and Images.
e Clipboard. Lock: On or Off.ce Browser icon (wrench), iLinq icon, and m messages display.ball Functionality Status: Scroll, (Measurement and Analysis), Position, Scan Area Width and Tilt.
12
18
16
14
17
15
13
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Q 7 Monitor Display Tour
titution/Hospital Name, Date, Time, Operator ntification.tient Name, Patient Identification.oustic Output Readout Symbol (Probe Orientation Marker). The
mbol is reversed on flipped images. age Preview, zoom reference box: .ay/Color Bar.ne Gauge. CINE frame/Total # of CINE mes (28/51), Frame time/total loop time.
8. Measurement Summary Window.9. Image.10. Measurement. 11. Measurement Results Window.12. Probe Identifier. Exam Study.13. Imaging Parameters by Mode.14. Focal Zone.15. TGC would display here if preset (not shown on
the image).16. Body Pattern.
17. Depth18. Imag
Active19. Imag20. Caps21. Servi
syste22. Track
M&A Size,
1 32
6
5
4
10
8
9
7
11
19 222120
LOGI 7
B/M-M
Powe
Optimibeam Values
Dynam
Dynamconveradjusta
Focus
Increamovesthe becorreson the
NOTEand Fo
Virtua
On Linof view
Rejec
Selectamplifiamplitu
Frame
Tempohas thimage
er
ount of lateral smoothing.
sion
s low-level echoes associated with lectrical noise.
Image Optimize
intuitive representation of non-quantitative amics in vascular structures.
ity/PRI
e sample rate for the flow signal.
und On/Off
nd On views the anatomy roadmap; nd Off views flow information only.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
B/M ModeImage Optimize
ode Image Optimize
r Output
zes image quality and allows user to reduce intensity. 10% increments between 0-100%. greater than 0.1 are displayed.
ic Range
ic Range controls how echo intensities are ted to shades of gray, thereby increasing the ble range of contrast.
Number and Position
ses the number of transmit focal zones or the focal zone(s) so that you can tighten up am for a specific area. A graphic caret ponding to the focal zone position(s) appears right edge of the image.
: Push key to toggle between Focus Number cus Position.
l Convex
ear and Sector probes, provides a larger field in the far field.
tion
s a level below which echoes will not be ed (an echo must have a certain minimum de before it will be processed).
Average
ral filter that averages frames together. This e effect of presenting a smoother, softer .
Edge Enhance
Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures. Adjustments to M Mode's edge enhancement affects the M Mode only.
Colorize
Enables gray scale image colorization. To deactivate, reselect a Gray Map.
Gray Map
Determines how the echo intensity levels received are presented as shades of gray.
Rotation (Up/Down)
Rotates the image by selecting the value from the pop up menu.
Coded Excitation (CE)
Improves image resolution and penetration in the far field.
Frequency
Multi Frequency mode lets you downshift to the probe's next lowerfrequency or shift up to a higher frequency.
Line Density
Optimizes B Mode frame rate or spatial resolution for the best possible image.
B Soften
Affects am
Suppres
Eliminateacoustic/e
B Flow
Provides hemodyn
Sensitiv
Adjusts th
Backgro
BackgrouBackgrou
LOGI 8
B/M-M
Anato
Allowsimage
Swee
Chang
Full T
Expan
Displa
Changbetwee
B-Mo
Auto
Autombasedanatom
Zoom
Magnimagniimageadjaceall imaactivatzoom Zoom
y. Changes system parameters to best or a particular patient type.
ere is an inter-dependency between gray in, and dynamic range. If you change a sit gain and dynamic range settings.
Range. Affects the amount of gray scale n displayed.
ance. Better delineates the amount of arpness.
erage. Smooths the image by averaging ffects the amount of speckle reduction.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ode Image Optimize (continued)
mical M Mode
you to rotate or move the M line in order to difficult-to-reach anatomy.
p Speed
es the speed at which the timeline is swept.
imeline
ds display to full timeline display.
y Format
es the horizontal/vertical display layout n B-Mode and M-Mode.
de Control Panel Controls
Optimize
atic Tissue Optimization optimizes the image upon a specified Region of Interest (ROI) or
y within the display.
fies a zoom region of interest, which is fied to approximately the size of a full-sized . An un-zoomed reference image is displayed nt to the zoom window. The system adjusts ging parameters accordingly. Press to e/deactivate; rotate to increase/decrease factor. Use the Trackball to position the 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 Flow. Provides a more intuitive representation of non-quantitative hemodynamics in vascular structure.
Frequencoptimize f
Maps. Thmaps, gamap, revi
Dynamicinformatio
Edge Enhborder sh
Frame Avframes. A
LOGI 9
r Modeze
Color
Angle
Estimato the betweemeasu
Angle
Angle or the angle.Steer. DoppleAvailab
Basel
Adjustslower
pecific color map to be selected. After a has been made, the color bar displays the map.
od flow to be viewed from a different ve, i.e. red away (negative velocities) and rd (positive velocities). The real-time or age can be inverted.
ize
he number of samples gathered for a or flow vector.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Color Flow/DoppleImage Optimi
Flow/PW Doppler Image Optimize
Correct
tes the flow velocity in a direction at an angle Doppler vector by computing the angle n the Doppler vector and the flow to be red.
Steer/Fine Angle Steer
Steer slants the Color Flow region of interest Doppler M line to obtain a better Doppler Press Angle Steer to access Fine Angle Fine Angle Steer allows you to steer the r cursor left/right 10 and 20 degrees. le from the Doppler Mode Touch Panel.
ine
s the baseline to accommodate faster or blood flows to eliminate aliasing.
PRF/Wall Filter
Velocity scale determines pulse repetition frequency. If the sample volume gate range exceeds single gate PRF capability, the system automatically switches to high PRF mode. Multiple gates appear, and HPRF is indicated on the display.
Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement.
NOTE: Push key to toggle between PRF and Wall Filter.
Threshold
Threshold assigns the gray scale level at which color information stops.
Map
Allows a sselection resultant
Invert
Allows bloperspectiblue towafrozen im
Packet S
Controls tsingle col
LOGI 10
Color
Modif
Press
Trace
In Autodecrea
Trace
Select
Auto
Specif
Quick
Quickl
Samp
Sizes
Trace
Specif
Duple
DuplexDuplex
PW/C
AdjustColor F
ase motion artifact. Increase the PRF, ase the Wall Filter.
ate aliasing. Increase the PRF and lower ine.
us imaging. Ensure that you have he vascular exam category, select a pplication, select the appropriate probe for rficial structure, select two focal zones, depth to the anatomy to be imaged,
a low gain setting for gray scale, activate , maintain the PRF at a lower setting, and
Frame Averaging for more persistence.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Flow/PW Doppler Image Optimize (continued)
y Auto Calcs
to select desired Auto Calcs.
Sensitivity
Calcs, increase to pick up more signal or se to pick up less signal.
Direction
Above, Below, or Both.
Calcs
y Auto Calcs Off/Live/Frozen.
Angle
y adjusts the angle by 60 degrees.
le Volume Gate Length
the sample volume gate.
Method
y Max, Mean, or Off.
x
on: simultaneous B-Mode and PW Mode; off: toggle live B-Mode and PW via B Pause.
F Ratio
s the ratio between Spectral Doppler and low.
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.
Color Flow Control Panel Control
Scan Area. Toggles between the CFM ROI window size and position.
M/D Cursor. Activates the Doppler cursor.
Scanning Hints
Line Density. Trades frame rate for sensitivity and spatial resolution. If the frame rate is too slow, reduce the size of the region of interest, select a different line density setting, or reduce the packet size.
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.
To decreand incre
To eliminthe Basel
For venoselected tvenous avery supeadjust themaintain Color Flowincrease
LOGI 11
Basic Measurements/Calculations
Basic
NOTEfirst sc
Distan
1. Prdis
2. To(dide
3. Tofixac
4. Topo(tis
5. Tosyva
NOTE
NOTEfixed c
NOTEerase but no
erence/Area (Trace) Measurement
Measure twice; a trace caliper displays.sition the trace caliper at the start point, the Trackball. the trace start point, press Set. The trace r changes to an active caliper.ce the measurement area, move the ball around the anatomy. A dotted line
s the traced area.o erase the dotted line but not the trace ess Clear once. To clear the trace caliper urrent data measured, press Clear twice.
o erase the line (bit by bit) back from its int, move the Trackball or turn the
ontrol counterclockwise.
mplete the measurement, press Set. The m displays the circumference and the area measurement results window.efore you complete a measurement:
o erase the line (bit by bit) back from its urrent point, move the Trackball or turn the llipse control counterclockwise.o erase the dotted line but not the trace aliper, press Clear once.o clear the trace caliper and the current ata measured, press Clear twice.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Measurements
: The following instructions assume that you an the patient and then press Freeze.
ce and Tissue Depth Measurements
ess Measure once; an active caliper plays. position the active caliper at the start point stance) or the most anterior point (tissue pth), move the Trackball. fix the start point, press Set. The system es the first caliper and displays a second tive caliper. position the second active caliper at the end int (distance) or the most posterior point sue depth), move the Trackball.
complete the measurement, press Set. The stem displays the distance or tissue depth lue in the measurement results window.: Before you complete a measurement:
To toggle between active calipers, press Measure.To erase the second caliper and the current data measured and start the measurement again, press Clear once.
: To rotate through and activate previously alipers, turn Cursor Select.
: After you complete the measurement, to all data that has been measured to this point, t data entered onto worksheets, press Clear.
Circumference/Area (Ellipse) Measurement
1. Press Measure once; an active caliper displays.
2. To position the active caliper, move the Trackball.
3. To fix the start point, press Set. The system fixes the first caliper and displays a second active caliper.
4. To position the second caliper, move the Trackball.
5. Turn the Ellipse control; an ellipse with an initial circle shape appears.
NOTE: Be careful not to press the Ellipse control as this activates the Body Pattern.
6. To position the ellipse and to size the measured axes (move the calipers), move the Trackball.
7. To increase the size, turn the Ellipse control in a clockwise direction. To decrease the size, turn the Ellipse control in a counterclockwise direction.
8. To toggle between active calipers, press Measure.
9. To complete the measurement, press Set. The system displays the circumference and area in the measurement results window.
NOTE: Before you complete a measurement:
To erase the ellipse and the current data measured, press Clear once. The original caliper is displayed to restart the measurement.To exit the measurement function without completing the measurement, press Clear a second time.
Circumf
1. Press2. To po
move3. To fix
calipe4. To tra
Trackshow
NOTE: Tcaliper, prand the c
NOTE: Tcurrent poEllipse c
5. To cosystein the
NOTE: B
TcETcTd
LOGI 12
Volum
1. Tofol
• Ma• Ma• Ma
NOdumepla
• Mame
• Ma2. Se
Time
1. Prve
2. Tomo
3. Tofixac
4. Tomo
5. Tosytwwi
eets
ent/Calculation worksheets are available and edit measurements and calculations. generic worksheets as well as n specific worksheets. The worksheets
ted from the Measurement Touch Panel.
re is not currently available.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
e
make a volume calculation, do one of the lowing:ke one distance measurement.ke two distance measurements.ke three distance measurements.TE: Three distances should be done in the
al format mode (side by side images). One asurement is usually made in the sagittal ne and two measurements in the axial plane.
ke one distance and one ellipse asurement.ke one ellipse measurement.lect Volume.
Interval Measurement
ess Measure twice; and active caliper with a rtical dotted line displays. position the active caliper at the start point, ve the Trackball.
fix the start point, press Set. The system es the first caliper and displays a second tive caliper. position the second caliper at the end point, ve the Trackball.
complete the measurement, press Set. The stem displays the time interval between the o calipers in the measurement results ndow.
Velocity Measurement
1. Press Measure; an active caliper with a vertical dotted line displays.
2. To position the caliper at the desired measurement point, move the Trackball.
3. To complete the measurement, press Set. The system displays the velocity measurement in the measurement results window.
PI, RI, S/D Ratio, D/S Ratio or A/B Ratio
Select PI, RI, S/D Ratio, A/B Ratio or D/S Ratio from the Doppler 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 S/D ratio, "A" velocity for A/B ratio or diastole for D/S ratio.
2. The second caliper is the end-point caliper to the end point of the Doppler waveform. This would be Vd for PI, minimum velocity for RI, diastole for S/D ratio, "B" velocity for A/B ratio or systole for D/S ratio.
NOTE: For the PI calculation, if Trace Auto is not selected, manually trace the waveform between VMAX and Vd.
NOTE: For the PI calculation, if Trace Auto is on, the system automatically traces the waveform when Set is pressed to fix Vd.
Worksh
Measuremto displayThere areApplicatioare selec
Reports
This featu
LOGI 13
Using
Conn
1. Plasu
2. Capro
3. DOImirre
4. Tu
5. Alica
6. Tuse
7. Cacores
re that the probe is placed gently in the holder.
ecting the probe
n be disconnected at any time. However, should not be selected as the active
the probe locking handle erclockwise. Pull the probe and connector ht out of the probe port.ully slide the probe and connector away the probe port and around the right side of yboard. Ensure the cable is free. re that the probe head is clean before g the probe in its storage box.
3S 10S
X X
X
X
X
X
X
X X
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Using Probes
Probes
ecting a probe
ce the probe's carrying case on a stable rface and open the case.refully remove the probe and unwrap the be cable. NOT allow the probe head to hang free.
pact to the probe head could result in parable damage.
rn the connector locking handle clockwise.
gn the connector with the probe port and refully push into place.rn the connector locking handle clockwise to cure the probe connector.refully position the probe cable in the probe rd holder spot so it is free to move, but not ting on the floor.
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.
Deactivating the probe
When deactivating the probe, the probe is automatically placed in standby mode.
1. Press the Freeze key.2. Gently wipe the excess gel from the face of the
probe. 3. Carefully slide the probe around the right side
of the keyboard, toward the probe holder.
Ensuprobe
Disconn
Probes cathe probeprobe.
1. Movecountstraig
2. Careffrom the ke
3. Be suplacin
Table 1-1: Probe Indications for Use
Probe Application 3C 3.5C 5C M7C E8C 7L 10L i12L M12L
Abdomen X X X X X X
Small Parts X X X X X X X
Periph. Vasc. X X X X X X
OB/GYN X X X X X X
Pediatrics X X X X X X
Neonatal X X X
Urology X X X X X X
Surgery X X
Endocavity X
Transcranial
Cardiac
LOGI 14
Prob
Pro 3S 10S P2D P6D
Coded
Coded X
B-Flow
Coded
LOGIQ X X
Virtual X
Easy 3 X X
Advan X X
Anatom X X
M Colo X X
TruAcc X X
Biopsy
Non-Im X X
Q 7 Quick Guide Direction 2291859-100 Rev. 1
e FeaturesTable 1-2: Probe Features
be Feature 3C 3.5C 5C M7C E8C 7L 10L i12L M12L
Excitation X
Harmonics X X X X X X
X
Contrast X
View X X X X X X X X X
Convex X X X X
D X X X X X X X X X
ced 3D X X X X X X X X X
ical M Mode X X X X X X X X X
r Flow X X X X X X X X
ess X X X X X X X X X
X X X X X X X X
aging CW
LOGI 15
Prob
Probe
when handling and protect from damage when not equipment damage.
ollow these precautions can result in serious injury
nector or probe adapters into any liquid.
drogen peroxide
damaged or defective probe.
t user to verify and maintain the effectiveness of the e procedures.
Probes for neuro surgical use must not be sterilized
oroughly clean the probe, as described on the
disinfecting means.
e solution:e probe connector or probe adaptors into any liquid.age such as cracks or chips in the housing may
orough inspection should be conducted during the
o the service manual for leakage check procedures.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Using Probes
e Cleaning and Disinfection Instructions
Safety
WARNING Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use carein use. DO NOT use a damaged or defective probe. Failure to follow these precautions can result in serious injury and
Ultrasound transducers can easily be damaged by improper handling and by contact with certain chemicals. Failure to fand equipment damage.• Do not immerse the probe into any liquid beyond the level specified for that probe. Never immerse the transducer con• Avoid mechanical shock or impact to the transducer and do not apply excessive bending or pulling force to the cable.• Transducer damage can result from contact with inappropriate coupling or cleaning agents:
• Do not soak or saturate transducers with solutions containing alcohol, bleach, ammonium chloride compounds or hy• Avoid contact with solutions or coupling gels containing mineral oil or lanolin• Avoid temperatures above 60°C.• Inspect the probe prior to use for damage or degeneration to the housing, strain relief, lens and seal. Do not use a
BiologicalHazard
CAUTION Adequate cleaning and disinfection are necessary to prevent disease transmission. It is the responsibility of the equipmeninfection control procedures in use. Always use sterile, legally marketed probe sheaths for intra-cavitary and intra-operativ
For neurological intra-operative procedures, use of a legally marketed, sterile, pyrogen free probe sheath is REQUIRED. with liquid chemical sterilants because of the possibility of neuro toxic residues remaining on the probe.
A defective probe or excessive force can cause patient injury or probe damage:• Observe depth markings and do not apply excessive force when inserting or manipulating intercavity probes.• Inspect probes for sharp edges or rough surfaces that could injure sensitive tissue.
In order for liquid chemical germicides to be effective, all visible residue must be removed during the cleaning process. Thfollowing page before attempting disinfection.
CREUTZFIELD-JACOB DISEASE Neurological use on patients with this disease must be avoided. If a probe becomes contaminated, there is no adequate
Electrical Hazard
The probe is driven with electrical energy that can injure the patient or user if live internal parts are contacted by conductiv• DO NOT immerse the probe into any liquid beyond the level indicated by the immersion level diagram. Never immerse th• DO NOT drop the probes or subject them to other types of mechanical shock or impact. Degraded performance or dam
result.• Inspect the probe before and after each use for damage or degradation to the housing, strain relief, lens, and seal. A th
cleaning process.• DO NOT kink, tightly coil, or apply excessive force on the probe cable. Insulation failure may result.• Electrical leakage checks should be performed on a routine basis by GE Service or qualified hospital personnel. Refer t
LOGI 16
Probe
1. Diremwi
2. Wawaspresso(suma
3. Riwa
4. Air
Probe
1. Prmapre
2. Plawigeis reqprorecPrmustetoxNeuspro
3. Afprorinres
isinfection Agents
ing high level disinfectant agents have roved for use with all probes:
OPA
s has been approved for the 8C probe.
high level disinfectant has been approved , 10L, 12L, 4S, 8C, and E8C probes.
high level disinfectant has been for the 7L, 10L, 12L, M7C, M12L, and es.
ing low level disinfect agents have been for use with all probes:
ac BluCloth HB (Wipes)
nd T-Spray II low level disinfectant has roved for the 7L, 10L, 12L, M7C, M12L, 8C probes.
6 low level disinfectant has been for the 7L, 10L, 12L, M7C, M12L, and es.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Cleaning, After Each Use
sconnect probe from ultrasound console and ove all coupling gel from probe by wiping
th a soft cloth and rinsing with flowing water. sh the probe with mild soap in lukewarm ter. Scrub the probe as needed using a soft onge, gauze, or cloth to remove all visible idue from the probe surface. Prolonged
aking or scrubbing with a soft bristle brush ch as a toothbrush) may be necessary if terial has dried onto the probe surface.
nse the probe with enough clean potable ter to remove all visible soap residue. dry or dry with a soft cloth.
Disinfection, After Each Use
epare the germicide solution according to the nufacturer's instructions. Be sure to follow all cautions for storage, use and disposal.ce the cleaned and dried probe in contact
th the germicide for the time specified by the rmicide manufacturer. High-level disinfection recommended for surface probes and is uired for endocavitary and intraoperative bes (follow the germicide manufacturer's ommended time).
obes for neuro surgical intra-operative use st NOT be sterilized with liquid chemical rilants because of the possibility of neuro ic residues remaining on the probe. urological procedures must be done with the e of legally marketed, sterile, pyrogen free be sheaths.
ter removing from the germicide, rinse the be following the germicide manufacturer's
sing instructions. Flush all visible germicide idue from the probe and allow to air dry.
Probe Immersion Levels
1. Fluid Level2. Aperture3. Contact face within patient environment
Probe D
The followbeen app
• Cidex• Cidex
Cidex Plu
Sporox II for the 7L
Pera SafeapprovedE8C prob
The followapproved
• Ster B• Sani-
T-Spray abeen app4S, and E
Virex II 25approvedE8C prob
1 2 3
3C3.5C5C
M7C E8C
7L10L M12L
3S10S P2D
P6D
i12L
LOGI 17
Imag
Clipb
As imakeys (PbottomthumbTheseof the
Printi
Press For mobutton
Brow
‘MouseSet to
Mana
From tNew P
Deleti
Selectonscre
Or, goof the be delfrom th
Up Patient Information
CD/MOD prior to following these steps.
t the Utility tab on the Touch Panel. Select m, then Backup/Restore.
t everything under Backup by placing a mark in front of Patient Archive, Report
ve, and User Defined Configuration. Then Backup. er ‘Ok’ to the Back-Up pop-up message ny times as the number of items you are
ng up.he detailed section of this menu s the user defined configuration above. s you to selectively restore what you want across multiple machines.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Image/ Patient Management and Connectivity
e Management
oard
ges are saved by pressing any of the print 1, P2, P3, or P4), the images appear at the
of the display on the clipboard as nails of the images saved during the exam. images remain on the clipboard until the end exam.
ng Images
the appropriate print key (P1, P2, P3, or P4). re information on programming the Print
s, See “Buttons” on page 21.
sing an Exam’s Stored Images
over’ the image in the clipboard, then press view an enlarged thumbnail image.
ging an Exam’s Stored Images
he Display, press Active Images; from the atient menu, open Active Images.
ng an Image
the image on the clipboard, then press the en Delete shortcut.
to Active Images (lower, right-hand portion display). Highlight all the images that need to eted and press Delete All Temp Images e Touch Panel
Formatting a CD/MOD
1. Insert the backup media. Format the backup media, CD-ROM or MOD. Select the Utility tab on the Touch Panel. Select Connectivity, then Tools. Label the media appropriately. Press Format.
2. The Ultrasound system displays a pop-up menu when the formatting has been completed. Press Ok to continue. Verify that the format was successful.
Backing
Format a
1. SelecSyste
2. SeleccheckArchipress
3. Answas mabacki
NOTE: TdecoupleThis allowto restore
LOGI 18
SavinLoops
Forma
1. Prtheme
2. SppreMO
3. Wonto
4. Finis
NOTEselect
the From Date, then press Recalculate. ify to Keep days together. Check that you enough disk space for the images you to move. If not, revise the move criteria. t Move Images, then press OK. An in-ess message appears. The archive tion is complete when you receive this age.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
g Images as JPEG files and CINE as AVI files
t a CD/MOD prior to following these steps.
ess Menu (on the lower, right-hand portion of display) and select Save As. The SAVE AS nu appears.
ecify Compression and Save As Type and ss Save. The image is saved to the CD/D.
hen you have saved all the images you want the CD/MOD, remove the media (press F3 eject the CD-ROM).
alize the CD by selecting Yes. The CD-ROM ejected from the system.
: If you want to add more images to the CD, “No” and do not finalize the CD.
Moving (Archiving) Images
Format a CD/MOD prior to following these steps.
1. Insert the backup media. Press Patient. Press More, then select Move Images. The Move Images pop-up appears.
2. Fill inSpechave want Selecprogroperamess
LOGI 19
Expor
Forma
1. Prin Prco
2. SemeupPa
3. In meNOse
NOwhof pa
4. OnexCo
5. Infcoup
6. Prejethe
tivity
ity on the LOGIQ 7 is based on the concept.
Concept
is a set of pre-configured services. For DICOM services may be for storage, erify, etc. In addition, there are other pes like video print, standard color print, local hard drive, select patient from local
, etc.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Image/ Patient Management and Connectivity
ting Patient Data
t a CD/MOD prior to following these steps.
ess Patient. Deselect any selected patient(s) the search portion of the Patient screen. ess More (located at the lower, right-hand rner of the Patient menu). lect Export. Specify the type of removable dia (MOD or CD-ROM) on the Export pop-
. Press OK. Then, please wait until the tient menu is visible.
the patient list at the bottom of the Patient nu, select the patient(s) you want to export. TE: You can use Windows commands to
lect more than one patient.
TE: You need to use your best judgment en moving patients’ images. If there are lots images or loops, then only move a few tients at a time.
ce you have selected all of the patients to port, press Copy Patient from the Select All/py Patient Menu. ormational status messages appear as the py is taking place. A final status report pop- message appears. Press OK. ess F3 to eject the CD or press the MOD ct button. Specify that you want to finalize CD-ROM.
Importing Patient Data/Images
1. At another Ultrasound system, insert the MOD or CD-ROM.
2. Press Patient, press More, then Import. The Import From pop-up message appears. Press OK.
3. The Patient menu just shows the patients available for import from the removable media you just loaded onto the system.
4. Select the patients to be imported. 5. Press Copy Patient from the Select All/Copy
Patient menu. 6. Please wait for the patient information to be
copied to this Ultrasound system. Informational messages appear while the import is taking place.
7. Press F3 to eject the media.
Connec
ConnectivDataflow
Dataflow
A dataflowexample,worklist, vservice tystorage todatabase
LOGI 20
Conf
Login Selectfrom ri
TCP/I
Type inAE Titlof the Mask,
(better known as Destinations)
t the Server from the pull-down menu. Add. t all the services for this device from the own menu to the right. Add. bottom of the menu, fill in the appropriate
ia for this service. Repeat this step for selected service for this device.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
iguring Connectivity
as Administrator. Press the left Utility tab. the Connectivity tab. Configure the menus ght to left, starting with TCP/IP first.
P
the Computer’s Name (better known as the e). Identify the Ultrasound system to the rest network by filling in its IP Address, Subnet and Gateway (if applicable). Press Save.
Services
1. Selec2. Press3. Selec
pull-d4. Press5. At the
critereach
LOGI 21
Butto
You cato a da
NOTEoutput
emember to specify each service Role as r Secondary. The primary service what always happens first to incoming or data. Only one primary role is available.
2
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Image/ Patient Management and Connectivity
ns
n assign print buttons (P1-P4) to a device or taflow.
: You can configure each print key to multiple devices/workflows.
Dataflow
Creates a Dataflow, (‘WL-LA-DServ -- Worklist, Local Archive, DICOM Server, for example).
1. Name the Dataflow (select from pull-down menu or add a new dataflow).
2. Configure the flow in the Services section of the screen. Select the Service from the pull-down menu and press Add.
NOTE: RPrimary ospecifies outgoing
1
LOGI 22
Verify
Select
a Device (DICOM Echo)
device, press Check.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ing a Device
the device, press DICOM Verify.
Views
Views a snapshot of this ultrasound system’s connectivity architecture (onboard network + external network + dataflows).
Pinging
Select the
LOGI 23
DICO
To cheDICOM
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Image/ Patient Management and Connectivity
M Status
ck the status of all DICOM jobs or redirect jobs, press F4.
LOGI 24
Using
Activa
Press CINE. Stop. T
To actiScan ACINE.
Quick
Press Last to
ecting B-Mode CINE from Timeline
the B-Mode CINE Loop only, press Cine lection and select B Only.
the Timeline CINE Loop only, press Cine lection and select TL Only.
to linked B-Mode and Timeline CINE Loop ess Cine Mode Selection and select
through a CINE Loop Frame By
e by Frame to move through CINE ne frame at a time.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
CINE
ting CINE
Freeze, then roll the Trackball to activate To start CINE Loop playback, press Run/o stop CINE Loop playback. press Run/Stop.
vate Timeline CINE, press Freeze, press rea, then roll the Trackball to activate
ly Move to Start/End Frame
First to move to the first CINE frame; press move to the last CINE frame.
Start Frame/End Frame
Turn the Start Frame dial to the left to move to the beginning of the CINE Loop. Turn the dial to the right to move forward through the CINE Loop.
Turn the End Frame dial to the right to move to the end of the CINE Loop. Turn the dial to the left to move backward through the CINE Loop.
Adjusting the CINE Loop Playback Speed
Turn the Loop Speed dial clockwise/counter-clockwise to increase/decrease the CINE Loop playback speed.
DisconnCINE
To reviewMode Se
To reviewMode Se
To return review, prB/TL.
Moving Frame
Turn Frammemory o
LOGI 25
Easy
Acqu
1. Opco
2. Prap
3. Tolef
4. Topeon
5. Thrig
NOTEscanniagain.
6. Tosc
ing a Surface Render
3D Touch Panel, press 3D, then press n the next Touch Panel to add a istic/clay-like quality to the render.
opacity and density via Threshold/press the key to adjust opacity). This hat ‘grays’ the system recognizes, ou to emphasize/de-emphasize grays as
y.
ay portions of the anatomy,
Scalpel. A caliper appears on the 3D
Set to set the caliper. Trackball around ortion to be cut away. le click and apply the scalpel. ge the projection and scalpel again.
ou can undo one scalpel, then check side of monitor.
Scanning Hints
propriate values for the 3D Acq Mode Plane.
able to set the scan distance before the ins.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Post Processing
3D
iring a 3D Scan
timize the B-Mode image. Ensure even gel verage. ess the 3D control panel key. Two screens pear. start acquiring the 3D image, press ‘L’ (the t split screen key). perform a parallel scan, scan evenly. To rform a sweep (fan) scan, rock the probe ce. Note the distance of the scan. e 3D volume of interest is generated on the ht side of the screen in real time.
: If the image stops before you’re done ng, start acquiring the 3D volume of interest
stop the 3D scan, press ‘R’ (the right split reen key).
Manipulating the 3D Scan
Imagine you are able to manipulate the 3D volume of interest (VOI) in your hand.
You can rotate it left to right or right to left. You can rotate it forward/backward (white hand).
Then, imagine that you can view the volume of interest one slice at a time through the anatomy (red hand).
Also imagine that you are able to pull back tissue to view specific portions of anatomy (yellow and green hands).
The 3D volume of interest is a tangible anatomical object that you can see and manipulate easily using the Trackball and Set control panel keys.
Practice positioning the pointer at different places within the 3D volume of interest. Highlight different colors, press Set to select this volume for manipulation. Use the hand to move the 3D volume.
Adjusting the 3D Volume of Interest
You can colorize the 3D volume of interest.
You can resize the VOI by adjusting the scan distance.
Perform
From the Texture ophotoreal
Adjust theOpacity (adjusts wallowing ynecessar
Scalpel
To cut aw
1. PressVOI.
2. Pressthe p
3. Doub4. Chan
NOTE: Yapply on
3DView
Set the apand Scan
It is advisscan beg
LOGI 26
Cont
INTER
http://w
USA
GE MeUltraso4855 WMilwauTEL: (
Clinic
For infMexicoCustomTEL: (In otheSales
Servic
For seTEL: (
Acces
To reqequipmRespoIn otheSales
al Systems Asiaort Centerkura cho, Hachiouji-shi2-0033) 426-48-2940 -- FAX: (81) 426-48-2905
INA
A.237ires - 140739-1619 -- FAX: (1) 567-2678
bH Medical Systems Austria en Strasse 8/8 IEN
3140 8459 toll free -- FAX: +43 1 505 38 74
al Systems Beneluxdestraat 3 OMMELGEM 0 11733 toll free 0 3 320 12 5922
as Médicosde Julho 52297 São Paulo SP0-122345 -- FAX: (011) 3067-8298
Q 7 Quick Guide Direction 2291859-100 Rev. 1
act Information
NET
ww.gemedicalsystems.com
dical Systemsund Service Engineering. Electric Avenuekee, WI 53219
1) 800-437-1171 or FAX: (1) 414-647-4090
al Questions
ormation in the United States, Canada, and parts of the Caribbean, call the er Answer Center:
1) 800-682-5327 or (1) 262-524-5698r locations, contact your local Applications, or Service Representative.
e Questions
rvice in the United States, call GE CARES 1) 800-437-1171
sories Catalog Requests
uest the latest GE Accessories catalog or ent brochures in the United States, call the
nse Center: TEL: (1) 800-643-6439r locations, contact your local Applications, or Service Representative.
Placing an Order
To place an order, order supplies or ask an accesory-related question in the United States, call the GE Access Center: TEL: (1) 800-472-3666In other locations, contact your local Applications, Sales or Service Representative.
OTHER COUNTRIES
NO TOLL FREE TEL: international code + 33 1 39 20 0007
CANADA
GE Medical SystemsUltrasound Svc Engineering TEL: (1) 800-664-07324855 W. Electric AvenueMilwaukee, WI 53219Customer Answer Center TEL: (1) 262-524-5698
LATIN & SOUTH AMERICA
GE Medical SystemsUltrasound Svc Engineering TEL: (1) 305-735-23044855 W. Electric AvenueMilwaukee, WI 53219Customer Answer Center TEL: (1) 262-524-5698
EUROPE
GE Ultraschall Deutschland GmbH & Co. KGBeethovenstraße 239Postfach 11 05 60D-42655 Solingen -- TEL: 0130 81 6370 toll freeTEL: (49) 212.28.02.207 -- FAX: (49) 212.28.02.431
ASIA
GE MedicAsia Supp67-4 TakaTokyo, 19TEL: (81
ARGENT
GEME S.Miranda 5Buenos ATEL: (1) 6
AUSTRIA
GE GesmPrinz EugA-1040 WTLX: 136TEL: 066
BELGIUM
GE MedicGulkenroB-2160 WTEL: 0 80FAX: +32TLX: 727
BRAZIL
GE SistemAv Nove 01407-90TEL: 080
LOGI 27
tion
DENM
GE MeFabrikDK-26TEL: +
FRAN
GE Me738 ruF-9265TEL: 0
GERM
GE UltDeutscBeethoPostfaD-426TEL: 0TEL: (
GREE
GE Me41, NikG-171TEL: +
ITALY
GE MeVia MoI-2005TEL: 1TLX: 3
al Systems España rturo Gimeno
Industrial ITORREJON DE ARDOZ95 3349 free -- FAX: +34 1 675 336484 A/B GEMDE
N
al Systems1243KISTA 795 433 toll free -- FAX: +46 87 51 30 9028 CGRSWES
LAND
al Systems (Schweiz) AG tweg 1KRIENS 5306 -- FAX: +41 41 421859
Sys. Turkiye A.S. ehliran Sodakn, No 24 Kat 1peL 212 75 5552 -- FAX: +90 212 211 2571
KINGDOM
al SystemsHouseingham Avenue
SL1 4ER0 89 7905 toll free -- FAX: +44 753 696067
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Contact Informa
ARK
dical Systems sparken 20 00 GLOSTRUP45 4348 5400 -- FAX: +45 4348 5399
CE
dical Systems e Yves Carmen 8 BOULOGNE CEDEX5 49 33 71 toll free -- FAX: +33 1 46 10 01 20
ANY
raschallhland GmbH & Co. KGvenstraße 239
ch 11 05 6055 Solingen130 81 6370 toll free49) 212.28.02.207 -- FAX: (49) 212.28.02.431
CE
dical Systems Hellasolaou Plastira Street
21 NEA SMYRNI30 1 93 24 582 -- FAX: +30 1 93 58 414
dical Systems Italiante Albenza 92 MONZA 678 744 73 toll free -- FAX: +39 39 73 37 86333 28
LUXEMBOURG
TEL: 0800 2603 toll free
MEXICO
GE Sistemas Médicos de Mexico S.A. de C.V.Rio Lerma #302, 1º y 2º PisosColonia Cuauhtémoc06500-México, D.F.TEL: (5) 228-9600 -- FAX: (5) 211-4631
NETHERLANDS
GE Medical Systems Nederland B.V. Atoomweg 512 NL-3542 AB UTRECHTTEL: 06 022 3797 toll free -- FAX: +31 304 11702
POLAND
GE Medical Systems PolskaKrzywickiego 34P-02-078 WARSZAWATEL: +48 2 625 59 62 -- FAX: +48 2 615 59 66
PORTUGAL
GE Medical Systems Portuguesa S.A.Rua Sa da Bandeira, 585Apartado 4094 TLX: 22804P-4002 PORTO CODEXTEL: 05 05 33 7313 toll free - FAX: +351 2 2084494
RUSSIA
GE VNIIEMMantulinskaya UI. 5A123100 MOSCOW TEL: +7 095 956 7037 -- FAX: +7 502 220 32 59TLX: 613020 GEMED SU
SPAIN
GE MedicHierro 1 APoligono E-28850 TEL:900 TLX: 223
SWEDE
GE MedicPO-BOX S-16428 TEL: 020TLX: 122
SWITZER
GE MedicSternmatCH-6010 TEL: 155
TURKEY
GE Med. Mevluk PYilmaz HaGayrettepISTANBUTEL: +90
UNITED
GE MedicCoolidge 352 BuckSLOUGHBerkshireTEL: 080
LOGI 28
Pape
Introd
Docum
• Re• Qu• On• CD
a PCuinc
• • • • • •
NOTEmultipl
ng Through Help
lp is organized like a manual, with chapters, sections, and pages.
he plus (+) sign next to MANUAL to open ok.
he plus sign next to the chapter you want open up that chapter.
he plus sign next to the chapter you want open up that section.
pen up the page to view that page’s n.
underlined text links you to related topics. he link to move to the new topic.
k to the previous screen, press Back. To he link, press Forward.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
rless Documentation
uction
entation is being provided via:
lease Notes (supplied on paper)ick Guide (supplied on paper)line Help (on the Ultrasound Scanner via F1)-ROM. You can view user documentation on C or on the Ultrasound Scanner via the stomer Documentation CD-ROM, which ludes:
Basic User ManualAdvanced Reference ManualQuick GuideQuick Card(s)Release Notes and WorkaroundsBasic Service Manual
: All user documentation is provided in e languages on the CD-ROM.
Using Online Help Via F1
Online Help is available via the F1 key.
The Help screen is divided into three sections:
• navigational tools on the top, left portion of the screen (Hide, Back, Forward)
• help book navigational tools on the left portion of the screen (Contents, Index, Search, Favorites)
• content portion on the right side of the screen where help topics are displayed
Navigati
Online Heindividual
Click on tup the bo
Click on tto view to
Click on tto view to
Click to oinformatio
The blue,Click on t
To go bacreturn to t
LOGI 29
Electronic Documentation
Help L
After ythe scr
Searc
To seatab. Tykeywophrasedisplaywant toDispla
e Help Index
n look for topics by using the Index. Press tab, then use the scroll bar to look up a
elp Features
e left side of the screen, press the Hide upper, left-hand portion of the screen. To
eft side of the screen again, press the n at the upper, left-hand portion of the
e Help window, position and hold down r at the corner of the screen while moving ball.
the Help window to the Touch Panel osition and hold down the cursor at the f the Help window while moving the
to the Touch Panel display.
nline Help
line Help, press the ‘X’ in the upper, right-er of the Online Help window.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
inks
ou click on a blue, underlined portion of text, een updates with this link’s content.
hing for a Topic in Help
rch for a specific topic, click on the Search pe in the topic name in the Type in the rd to find: field. Topics with the word or you typed appear in the Select Topic to : area. Either double click on the topic you view or highlight the topic and press the
y button to view this topic.
Creating a List of Favorite Topics in Help
You may find that there are topics you need to refer to often. In this case, it’s a good idea to save these topics as Favorites. To save a topic as a favorite, press the Favorites tab, highlight the topic in the Topics window, and press the Add button. You can now view this topic quickly by going to the Favorites help tab.
Using th
Or, you cathe Indextopic.
Other H
To hide thicon at theview the lShow icoscreen.
To size ththe cursothe Track
To move display, pvery top oTrackball
Exiting O
To exit Onhand corn
LOGI 30
Acces
To view
1. Ins2. Op3. Do
do4. Se
blu
To closright-h
NOTEAcrobaCD. O‘ar505Acroba
t Scanner Utilities.
t Scanner Documentation Interface. l to find the document, double click on the
ent, and open it. ou can search through a document, use s in the Table of Contents and Index to ics, and navigate via bookmarks.
addition to viewing documentation on the d system, the Documentation CD can be ny PC.
ess the ‘X’ in the upper, right-hand corner umentation window.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
sing Documentation Via a PC
user documentation on a PC,
ert the CD into the CD drive. en the CD drive on your desktop. uble click on the ‘gedocumentation.html’ cument. lect the item you want to view (click on the e, underlined link in the File Name column).
e the window, click on the ‘X’ in the upper, and corner of the browser window.
: If your PC does not have the Adobe t Reader, the PC version is supplied on the
pen the CD and double click on enu.exe. Follow the prompts to install Adobe t Reader on your PC.
Accessing Documentation on the Ultrasound Scanner Via the CD-ROM
To access documentation via the CD-ROM,
1. Logon as ‘Operator’ next to Select User Level. Enter the following password: ‘uls’. Press Okay.
2. Press Utilities and insert the CD-ROM.
3. Selec
4. Selec5. Scrol
documNOTE: Yhyperlinklocate top
NOTE: InUltrasounread on a
To exit, prof the doc
LOGI 31
Preca
Icon d
Variou f the following flag words and icons which preced
NOTE ally:
• Ma• Us• No
s will cause:
s may cause:
or can cause:
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
ution Levels
escription
s levels of safety precautions may be found on the equipment and different levels of concern are identified by one oe the precautionary statement .
: Indicates precautions or recommendations that should be used in the operation of the ultrasound system, specific
intaining an optimum system environmenting this Manualtes to emphasize or clarify a point.
DANGER Indicates that a specific hazard is known to exist which through inappropriate conditions or action
• Severe or fatal personal injury• Substantial property damage.
WARNING Indicates that a specific hazard is known to exist which through inappropriate conditions or action
• Severe personal injury• Substantial property damage.
CAUTION Indicates that a potential hazard may exist which through inappropriate conditions or actions will
• Minor injury• Property damage.
LOGI 32
Haza
Potent
Usage Source
are instructionsve guidelines
ISO 7000No. 0659
back panel
of power output following easonably achievable
sthetic
ss
Q 7 Quick Guide Direction 2291859-100 Rev. 1
rd Symbols - Icon Description
ial hazards are indicated by the following icons:
Table 1-1: Potential Hazards
Icon Potential Hazard
BiologicalHazard
• Patient/user infection due to contaminated equipment. • Cleaning and c• Sheath and glo
Electrical Hazard
• Electrical micro-shock to patient, e.g., ventricular • Probes• ECG• Connections to
MovingHazard
• Console, accessories or optional storage devices that can fall on patient, user, or others.• Collision with persons or objects result in injury while maneuvering or during system
transport.• Injury to user from moving the console.
• Moving• Using brakes• Transporting
Acoustic Output Hazard
• Patient injury or tissue damage from ultrasound radiation. • ALARA, the usethe as low as rprinciple
Explosion Hazard
• Risk of explosion if used in the presence of flammable anesthetics. • Flammable ane
Smoke & Fire Hazard
• Patient/user injury or adverse reaction from fire or smoke.• Patient/use injury from explosion and fire.
• Replacing fuse• Outlet guideline
LOGI 33
Impor
The fo user aware of particular hazards associ nal precautions may be provided throug
Patie
Relate
Patien
Always entering such data. Make sure correct patient .
Diagn
Equipm The equipment user must become thorou . Applications training is available through the loc nce program.
ns and potential hazards involving GE Medical Systems if needed.
ld result in injury.
examination.
g the system to transmit acoustic output coustic output or freeze the image when
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
tant Safety Considerations
llowing topic headings (Patient Safety, and Equipment and Personnel Safety) are intended to make the equipment ated with the use of this equipment and the extent to which injury can occur if precautions are not observed. Additiohout the manual.
nt Safety
d Hazards
t identification
include proper identification with all patient data and verify the accuracy of the patient's name or ID numbers when ID is provided on all recorded data and hard copy prints. Identification errors could result in an incorrect diagnosis
ostic information
ent malfunction or incorrect settings can result in measurement errors or failure to detect details within the image.ghly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctionsal GE representative. Added confidence in the equipment operation can be gained by establishing a quality assura
CAUTION Improper use can result in serious injury. The user must be thoroughly familiar with the instructioultrasound examination before attempting to use the device. Training assistance is available from
The equipment user is obligated to be familiar with these concerns and avoid conditions that cou
WARNING The concerns listed can seriously affect the safety of patients undergoing a diagnostic ultrasound
CAUTION The system’s acoustic output remains transmitting when the user controls are being used. Allowinwith the probe not in use (or in its holder) can cause the probe to build up heat. Always turn off anot in use.
LOGI 34
Relate
Mecha
The us f infection. Inspect probes often for sharp, pointe nipulating intracavity probes. Become familia
Trainin
It is re contact the local GE representative for trainin
ALARA basic ultrasound principles, possible biologi e ALARA principle.
ct with internal live parts. Inspect probes mage that could allow liquid entry.
g. Take extra care not to drop e can result in patient injury or serious
inimize exposure time and keep asonably Achievable), increasing output familiar with all controls affecting the e Manual for more information.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
d Hazards (continued)
nical hazards
e of damaged probes or improper use and manipulation of intracavity probes can result in injury or increased risk od, or rough surface damage that could cause injury or tear protective barriers. Never use excessive force when mar with all instructions and precautions provided with special purpose probes.
g
commended that all users receive proper training in applications before performing them in a clinical setting. Pleaseg assistance.
training is provided by GE Application Specialists. The ALARA education program for the clinical end-user coverscal effects, the derivation and meaning of the indices, ALARA principles, and examples of specific applications of th
Electrical Hazard
A damaged probe can also increase the risk of electric shock if conductive solutions come in contaoften for cracks or openings in the housing and holes in and around the acoustic lens or other daBecome familiar with the probe's use and care precautions outlined in Probes and Biopsy.
CAUTION Ultrasound transducers are sensitive instruments which can easily be damaged by rough handlintransducers and avoid contact with sharp or abrasive surfaces. A damaged housing, lens or cablimpairment or operation.
CAUTION Ultrasound can produce harmful effects in tissue and potentially result in patient injury. Always multrasound levels low when there is no medical benefit. Use the principle of ALARA (As Low As Reonly when needed to obtain diagnostic image quality. Observe the acoustic output display and beoutput level. See the Bioeffects section of the Acoustic Output chapter in the Advanced Referenc
CAUTION Do not use with Defibrillator.
This equipment does not have a defibrillator approved applied part.
LOGI 35
Equip
Relate
proper action for the patient. Inform a
vice personnel only.
nd accessories must be securely
iagnostic ultrasound examination.
alified service personnel.unding outlet.
ins power plug. The protective earth
se the risk of shock.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
ment and Personnel Safety
d Hazards
WARNING This equipment contains dangerous voltages that are capable of serious injury or death.
If any defects are observed or malfunctions occur, stop operating the equipment and perform thequalified service person and contact a Service Representative for information.
There are no user serviceable components inside the console. Refer all servicing to qualified ser
WARNING Only approved and recommended peripherals and accessories should be used. All peripherals amounted to the LOGIQ 7.
DANGER The concerns listed below can seriously affect the safety of equipment and personnel during a d
Explosion Hazard
Risk of explosion if used in the presence of flammable anesthetics.
Electrical Hazard
To avoid injury:
• Do not remove protective covers. No user serviceable parts are inside. Refer servicing to qu• To assure adequate grounding, connect the attachment plug to a reliable (hospital grade) gro• Never use any adaptor or converter of a three-prong-to-two-prong type to connect with a ma
connection will loosen.• Do not place liquids on or above the console. Spilled liquid may contact live parts and increa
• Plug any peripherals into the LOGIQ 7 AC power outlet.
LOGI 36
Relate
rmance verified by qualified service
ply circuit must be as specified in
dures. To avoid the risk of disease
ures when appropriate.fect or sterilize as needed. Refer to
y apply to personnel and equipment.
to the natural latex protein. Sensitive atex content and FDA’s March 29, 1991
the image when the sytem is not in use.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
d Hazards (continued)
CAUTION Do not use this equipment if a safety problem is known to exist. Have the unit repaired and perfopersonnel before returning to use.
Smoke & Fire Hazard
The system must be supplied from an adequately rated electrical circuit. The capacity of the supChapter 3 of the Basic User Manual.
BiologicalHazard
For patient and personnel safety, be aware of biological hazards while performing invasive procetransmission:
• Use protective barriers (gloves and probe sheaths) whenever possible. Follow sterile proced• Thoroughly clean probes and reusable accessories after each patient examination and disin
Probes and Biopsy in the Basic User Manual for probe use and care instructions.• Follow all infection control policies established by your office, department or institution as the
CAUTION Contact with natural rubber latex may cause a severe anaphylactic reaction in persons sensitive users and patients must avoid contact with these items. Refer to package labeling to determine lMedical Alert on latex products.
CAUTION The system is equipped with an Auto Freeze feature which disables acoustic output and freezesTake care when deactivating this feature.
CAUTION Never put any device onto the monitor.
LOGI 37
Relate
mended on a daily basis.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
d Hazards (continued)
CAUTION Archived data is managed at the individual sites. Performing data backup (to any device) is recom
CAUTION Do not unpack the LOGIQ 7. This must be performed by qualified service personnel only.
CAUTION Do not use the LOGIQ 7 Ultrasound system ECG wave for diagnosis and monitoring.
LOGI 38
Devic
Label
The fo uipment.
Location
Identif See “Label Location (b)” on page 52.
Type/C
IP Cod Foot Switch
Probe connectors and PCG connector
ECG marked Type CF
Various
Inside of console
Refer to Chapter 3 in the Basic User Manual for location information.
Refer to Chapter 3 in the Basic User Manual for location information.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
e Labels
Icon Description
llowing table describes the purpose and location of safety labels and other important information provided on the eq
Table 1-2: Label Icons
Label/Icon Purpose/Meaning
ication and Rating Plate Manufacture’s name and addressDate of manufactureModel and serial numbersElectrical ratings (Volts, Amps, phase, and frequency)
lass Label Used to indicate the degree of safety or protection.
e (IPX8) Indicates the degree of protection provided by the enclosure per IEC60 529. Can be used in operating room environment.
Type BF Applied Part (man in the box) symbol is in accordance with IEC 878-02-03.
Type CF Applied Part (heart in the box) symbol is in accordance with IEC 878-02-03.
!“ATTENTION” - Consult accompanying documents” is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.
“CAUTION” - Dangerous voltage” (the lightning flash with arrowhead) is used to indicate electric shock hazards.
“Mains OFF” indicates the power off position of the mains power breaker.
“Mains ON” indicates the power on position of the mains power breaker.
LOGI 39
Refer to Chapter 3 in the Basic User Manual for location information.
Internal
Rear of console
Location
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
“ON” indicates the power on position of the power switch.CAUTION: This Power Switch DOES NOT ISOLATE Mains Supply.“Standby” indicates the power standby position of the power switch.CAUTION: This Power Switch DOES NOT ISOLATE Mains Supply.
“Protective Earth” indicates the protective earth (grounding) terminal.
“Equipotentiality” indicates the terminal to be used for connecting equipotential conductors when interconnecting (grounding) with other equipment.
Table 1-2: Label Icons
Label/Icon Purpose/Meaning
LOGI 40
Class
Type o
ClDegre
TyTy
Contin
System
Footsw
*1. Cl
EQUIP ground. This additional safety precaution preven
*2. Ty
TYPE able LEAKAGE CURRENT.
*3. Ty
Type C articularly regarding allowable LEAKAGE CURR
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ifications
f protection against electric shock
ass I Equipment (*1)e of protection against electric shock
pe BF Applied part (*2) (for PCG, Probes marked with BF symbol)pe CF Applied part (*3) (for ECG, Probes marked with CF symbol)uous Operation
is Ordinary Equipment (IPX0)
itch is IPX8
ass I EQUIPMENT
MENT in which protection against electric shock does not rely on BASIC INSULATION only, but includes an earth ts exposed metal parts from becoming LIVE in the event of an insulation failure.
pe BF APPLIED PART
BF APPLIED PART providing a specified degree of protection against electric shock, with particular regard to allow
pe CF APPLIED PART
F Applied Part providing a degree of protection higher than that for TYPE BF Applied Part against electric shock pENTS.
Table 1-3: Type BF Equipment
Normal Mode Single fault condition
Patient leakage current Less than 100 microA Less than 500 microA
Table 1-4: Type CF Equipment
Normal Mode Single fault condition
Patient leakage current Less than 10 microA Less than 50 microA
LOGI 41
EMC
NOTE ncy interference to other medical and non-medica plies with emissions limits for a Group 1, Class cur in a particular installation.
NOTE the user (or qualified service personnel) should
• reo• inc• po• coNOTE cables or by unauthorized changes or modific ipment.
NOTE to peripheral devices must be shielded and pr uency interference in violation of the FCC regula
NOTE ucts) in the vicinity of the equipment as it may ca ear this equipment.
The m und this equipment to fully comply with the above
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
(Electromagnetic Compatibility)
: This equipment generates, uses and can radiate radio frequency energy. The equipment may cause radio frequel devices and radio communications. To provide reasonable protection against such interference, this product com
A Medical Devices Directive as stated in EN 60601-1-2. However, there is no guarantee that interference will not oc
: If this equipment is found to cause interference (which may be determined by turning the equipment on and off), attempt to correct the problem by one or more of the following measure(s):
rient or relocate the affected device(s)rease the separation between the equipment and the affected devicewer the equipment from a source different from that of the affected devicensult the point of purchase or service representative for further suggestions.: The manufacturer is not responsible for any interference caused by using other than recommended interconnect ations to this equipment. Unauthorized changes or modifications could void the users’ authority to operate the equ
: To comply with the regulations on electromagnetic interference for a Class A FCC Device, all interconnect cablesoperly grounded. Use of cables not properly shielded and grounded may result in the equipment causing radio freqtions.
: Do not use devices which intentionally transmit RF Signals (cellular phones, transceivers, or radio-controlled produse performance outside the published specifications. Keep the power to these types of devices turned off when n
edical staff in charge of this equipment is required to instruct technicians, patients, and other people who maybe aro requirement.
LOGI 42
(cont
EMC
All typ ansmitted through air or connecting cables ce from other equipment and at the same time n
Proper
The pr
In case
The m by unauthorized changes or modifications to this
Portab r networks) should be used no closer to any pa
controlled products) in the vicinity of this these type devices turned off when near
ople who may be around this equipment
ents
800 MHz - 2.5 GHz
Calcul d = [7/E1] square root of P
Where ed RF
If th be
5 5.2
20 10.5
100 24.0
Q 7 Quick Guide Direction 2291859-100 Rev. 1
inued)
Performance
es of electronic equipment may characteristically cause electromagnetic interference with other equipment, either tr. The term EMC (Electromagnetic Compatibility) indicates the capability of equipment to curb electromagnetic influenot affect other equipment with similar electromagnetic radiation from itself.
installation following the service manual is required in order to achieve the full EMC performance of the product.
oduct must be installed as stipulated in 4.2, Notice upon Installation of Product.
of issues related to EMC, please call your service personnel.
anufacturer is not responsible for any interference caused by using other than recommended interconnect cables orequipment. Unauthorized changes or modifications could void the users’ authority to operate the equipment.
le and mobile radio communications equipment (e.g. two-way radio, cellular/cordless telephones, wireless computert of this system, including cables, than determined according to the following method:
CAUTION Do not use devices which intentionally transmit RF signals (cellular phones, transceivers, or radioequipment as it may cause performance outside the published specifications. Keep the power tothis equipment.
Keep power to these devices turned off when near this equipment.
Medical staff in charge of this equipment is required to instruct technicians, patients and other peto fully comply with the above regulation.
Table 1-5: Portable and mobile radio communications equipment distance requirem
Frequency Range: 150 kHz - 80 MHz 80 MHz - 800 MHz
ation Method: d=[3.5/V1] square root of P d = [3.5/E1] square root of P
: d= separation distance in meters, P = rated power of the transmitter, V1=compliance value for conducted RF, E1 = compliance value for radiat
e maximum transmitter power in watts is rated The separation distance in meters should
2.6 2.6
5.2 5.2
12.0 12.0
LOGI 43
Notic
Separa base stations for radio (cellular/cordless) teleph predicted theoretically with accuracy. To assess d. If the measured field strength in the locatio laration, the ultrasound system should be observ e-orienting or relocating the ultrasound system
1. Us ts equipped with a power source plug sh or converter to connect with a power so
2. Lo3. Be e installation procedures (i.e. wire power
ca4. La ation manuals.
Gene
1. DeTh ising its EMC performance.Av mance of the product.
2. NoThMoa.b.c.d.
3. Op uming operation.4. Op
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
e upon Installation of Product
tion distance and effect from fixed radio communications equipment: field strengths from fixed transmitters, such asones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast transmitter cannot be the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be consideren in which the ultrasound system is used exceeds the applicable RF compliance level as stated in the immunity deced to verify normal operation. If abnormal operation is observed, additional measures may be necessary, such as r or using an RF shielded examination room may be necessary.
e either power supply cords provided by GE Medical Systems or ones designated by GE Medical Systems. Producould be plugged into the fixed power socket which has the protective grounding conductor. Never use any adaptor urce plug (i.e. three-prong-to-two-prong converter).cate the equipment as far away as possible from other electronic equipment. sure to use only the cables provided by or designated by GE Medical Systems. Connect these cables following thbles separately from signal cables).y out the main equipment and other peripherals following the installation procedures described in the Option Install
ral Notice
signation of Peripheral Equipment Connectable to This Product.e equipment indicated on Chapter 15 of the Basic User Manual can be hooked up to the product without compromoid using equipment not designated in the list. Failure to comply with this instruction may result in poor EMC perfortice against User Modificatione user should never modify this product. User modifications may cause degradation in EMC performance.dification of the product includes changes in:Cables (length, material, wiring, etc.)System installation/layoutSystem configuration/componentsSecuring system parts (cover open/close, cover screwing)
erate the system with all covers closed. If a cover is opened for some reason, be sure to shut it before starting/reserating the system with any cover open may affect EMC performance.
LOGI 44
Perip
The fo LOGIQ 7 to image recording and other device
The LO ng devices:
• So• So• So• Mi• So• So• SoThe LO rear panel Ethernet connection, provided the LA
Conne ear panel.
The LO nd their specifications, installation, and interco
Gener
1. Th2. Th t be less than or equal to the rated supply
of 3. Th4. Th5. Ri6. Ele
Q 7 Quick Guide Direction 2291859-100 Rev. 1
heral Update for EC countries
llowing is intended to provide the users in EC countries with updated information concerning the connection of the s or communication networks.
GIQ 7 has been verified for overall safety, compatibility and compliance with the following on-board image recordi
ny UP 895 MDW B&W Video Printerny UP-21 MD Color Video Printerny UP-51MDU Color Video Printertsubishi 91W Color Video Printerny SVO-9500 MD2 S-VHS Video Cassette Recorder\ny UP-D895 B&W Digital Printerny UP-D21MD Color Digital PrinterGIQ 7 has also been verified for compatibility, and compliance for connection to a local area network (LAN) via the
N components are IEC/EN 60950 compliant.
ction may also be made to a CE Marked and IEC/EN 60950 compliant modem using one of the serial ports at the r
GIQ 7 may also be used safely while connected to devices other than those recommended above if the devices annection with the system conform to the requirements of IEC/EN 60601-1-1.
al precautions for installing an alternate on-board device would include:
e added device must have appropriate safety standard conformance and CE Marking.e total power consumption of the added devices, which connect to the LOGIQ 7 and are used simultaneously, musthe LOGIQ 7.ere must be adequate heat dissipation and ventilation to prevent overheating of the device.ere must be adequate mechanical mounting of the device and stability of the combination.sk and leakage current of the combination must comply with IEC/EN 60601-1.ctromagnetic emissions and immunity of the combination must conform to IEC/EN 60601-1-2.
LOGI 45
Perip
Gener
1. Th2. Th3. Sig 0601-1-1.
Decla
This sy tic environment as specified.
tions can result in an electric shock ification of compatibility and conformity to nd electromagnetic interference are the
Emi
CISPRRF Em
likely to cause any interference in nearby electronic y connected to the public low-voltage power supply rding to CISPR Class A/B.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
heral Update for EC countries (continued)
al precautions for installing an alternate off-board, remote device or a network would include:
e added device(s) must have appropriate safety standard conformance and CE Marking.e added device(s) must be used for their intended purpose having a compatible interface.nal or mains isolation devices and additional protective earth may be needed to assure compliance with IEC/EN 6
ration of Emissions
stem is suitable for use in the following environment. The user must assure that it is used only in the electromagne
CAUTION The connection of equipment or transmission networks other than as specified in the user instruchazard or equipment malfunction. Substitute or alternate equipment and connections requires verIEC/EN 60601-1-1 by the installer. Equipment modifications and possible resulting malfunctions aresponsibility of the owner.
Table 1-6: Declaration of Emissions
ssion Type Compliance Electromagnetic Environment
11 issions
Group 1 Class A
This system uses RF energy only for its internal function. Therefore, RF emissions are very low and are not equipment. It is suitable for use in all establishments, other than domestic establishments and those directlnetwork that supplies buildings used for domestic purposes. Note: Select only one underlined word(s) acco
LOGI 46
Decla
This sy e specified guidance and only in the electro
EMC Environment and Guidance
IEC 61Static (ESD)
uld be wood, concrete, or ceramic tile. If floors are ith synthetic material, the relative humidity should 30%.er quality should be that of a typical commercial pital environment. If the user requires continued
during power mains interruptions, it is ded that the system be powered from an table power source (UPS). is the a.c. mains voltage prior to application of the
uency magnetic fields should be at levels tic of a typical location in a typical commercial and/
environment. distance to radio communication equipment must ned according to the Table 1-5 on page 42. e may occur in the vicinity of equipment marked mbol
IEC 61Electritransie
IEC 61
IEC 61Voltagvoltag
IEC 61Powerfield
IEC 61Condu
IEC 61Radiat
NOTE and people.
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ration of Immunity
stem is suitable for use in the following environment. The user must assure that the system is used according to thmagnetic environment listed.
Table 1-7: Declaration of Immunity
Immunity Type Test Level Compliance
000-4-2discharge
± 8 kV contact
± 8 kV air
± 6 kV contact
± 8 kV air
Floors shocovered wbe at leastMains powand/or hosoperation recommenuninterrupNOTE: UTtest level.Power freqcharacterisor hospitalSeparationbe maintaiInterferencwith the sy
000-4-4cal fastnt/burst
± 1.5 kV for mains ± 2 kV for mains
± 1 kV for SIP/SOP
000-4-5 Surge Immunity ± 1.5 kV differential
± 2.5 kV common
± 1 kV differential
± 2 kV common
000-4-11e dips, short interruptions and e variations on mains supply
< 5% UT (> 95% dip) for 0.5 cycle; < 5% UT (> 95% dip) for 0.5 cycle;40% UT (60% dip) for 5 cycles;70% UT (30% dip) for 25 cycles;< 5% UT (>95% dip) for 5 sec
000-4-8 frequency (50/60 Hz) magnetic
TBD 3 A/m
000-4-6cted RF
TBD 3 VRMS150 kHz - 80 MHz
000-4-3ed RF
3 V/m80 MHz - 2.5 GHz
3 V/m80 MHz - 2.5 GHz
: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects,
LOGI 47
Patie
1. Pe2. Fr3. No4. Im5. Pr6. EC7. PC8. Ph9. Re
lephone Lineh
ne (AC~)ineble with Protective Earth
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
nt Environmental Devices
Figure 1-1. Patient Environmental Devices
ripheral Device (Signals I/O Port, Power In)ont Panel (Signal I/O Port, Power Out)n-Imaging Probesaging Probesobe PortG CableG Sensorysio-Signal Input Panelar Panel
10. Signals I/O Port11. Power Out12. Signals I/O Port13. Footswitch Connector14. Power In15. Peripheral Devices16. Signals I/O Port17. Power In18. InSite Modem (Signal I/O Port)
19. Power Te20. Footswitc21. Power Li22. Ground L23. Power Ca24. MO Drive25. CD-RW
12
3
45
86
7
9
10
11
15
16
17
12
1819
13
20
1421
2223
24
25
LOGI 48
Accep
The de NT ENVIRONMENT.
Unap
Acces
ONMENT.
low:
oved or recommended in these
Q 7 Quick Guide Direction 2291859-100 Rev. 1
table Devices
vices shown in “Patient Environmental Devices” on page 1-47 are specified to be suitable for use within the PATIE
proved Devices
sories, Options, Supplies
CAUTION DO NOT connect any probes or accessories without approval by GE within the PATIENT ENVIR
See “Peripheral Update for EC countries” on page 44.
CAUTION Unapproved devices shall not be used in the patient environment.
If devices are connected without the approval of GE, the warranty will be INVALID.
Any device connected to the LOGIQ 7 must conform to one or more of the requirements listed be
1. IEC standard or equivalent standards appropriate to devices.2. The devices shall be connected to PROTECTIVE EARTH (GROUND).
CAUTION Unsafe operation or malfunction may result. Use only the accessories, options and supplies apprinstructions for use.
LOGI 49
Acou
Locate al-time indication of acoustic levels being genera display is based on NEMA/AIUM Standa
Acou
The di . Although not part of the NEMA/AIUM standa on the examination and type of tissue involve
• So re increase in soft tissue.• Bo it provides an estimate of potential
tem• Cr es an estimate of potential temperature
inc
The TI ay precision is ± 0.1, and accuracy is ± 50%.
Contr
The po
The Ac
Indirec ffects portion of each control in the Modes chapte
Always
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
stic Output
d on the upper right section of the system display monitor, the acoustic output display provides the operator with reted by the system. See the Acoustic Output chapter in the Advanced Reference Manual for more information. Thisrds for Real-time Display of Thermal and Mechanic Acoustic Output Indices on Diagnostic Ultrasound Equipment.
stic Output Display Specifications
splay consists of three parts: Thermal Index (TI), Mechanical Index (MI), and a relative Acoustic Output (AO) valuerd, the AO value informs the user of where the system is operating within the range of available output. Dependingd, the TI parameter will be one of three types:
ft Tissue Thermal Index (TIS). Used when imaging soft tissue only, it provides an estimate of potential temperatune Thermal Index (TIB). Used when bone is near the focus of the image as in the third trimester OB examination,perature increase in the bone or adjacent soft tissue.
anial Bone Thermal Index (TIC). Used when bone is near the skin surface as in transcranial examination, it providrease in the bone or adjacent soft tissue.
and MI is displayed at all times. The MI and TI displays start at a value of 0.0 and increments in steps of 0.1. Displ
ols Affecting Output
tential for producing mechanical bioeffects (MI) or thermal bioeffects (TI) can be influenced by certain controls.
oustic Output control has the most significant effect on Acoustic Output.
t effects may occur when adjusting other controls. Controls that can influence MI and TI are detailed under the Bioer of the Basic User Manual.
observe the acoustic output display for possible effects.
LOGI 50
Best p
NOTE
Acou
In orde lt output level. This reduced level is preset progra or New Patient is selected.
ct on Acoustic Output, such as Gain and
to adjust the Acoustic Output control or
ring an examination. Begin the exam with
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ractices while scanning
: Refer to the Optimization sections of the Modes chapter for a complete discussion of each control.
stic Output Default Levels
r to assure that an exam may not start at a high output level, the LOGIQ 7 may initiate scanning at a reduced defaummable and depends upon the exam category and probe selected. It takes effect when the system is powered on
HINTS Raise the Acoustic Output only after attempting image optimization with controls that have no effeTGC.
WARNING Be sure to have read and understood control explanations for each Mode used before attemptingany control that can effect Acoustic Output.
Acoustic Output Hazard
Use the minimum necessary acoustic output to get the best diagnostic image or measurement duthe probe that provides an optimum focal depth and penetration.
LOGI 51
Warn
Cons
ion Explanations
s. No user serviceable parts are inside. Refer
ellular phone, radio receiver, mobile radio es near this equipment could cause this equipment ower to these devices turned off when near this
To avoid possible injury and equipment damage
clines or long distance.
nforms with the Council Directive 93/42/EEC.
oup 1, Class A of the international standard for
G”, NOT “PROTECTIVE EARTH”.
uipment is connected to a receptacle marked , Japan)
(8)
Q 7 Quick Guide Direction 2291859-100 Rev. 1
Safety
ing Label Locations
ole Labels
Figure 1-2. Label Location (a)
Table 1-8: Label Locat
1. Possible shock hazard. Do not remove covers or panelservicing to qualified service personnel.
2. Do not use the following devices near this equipment: ctransimitter, radio controlled toy, etc. Use of these devicto perform outside the published specifications. Keep pequipment.
3. The equipment weighs approximately 225 kg (496 lbs).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 in
4. Prescription Device (For U.S.A. Only)5. The CE Mark of Conformity indicates this equipment co6. CISPR
CAUTION: The LOGIQ 7 conforms to the CISPR11, GrElectromagnetic disturbance characteristics.
7. Voltage Range (Indication label)8. Signal ground point label
CAUTION: This is only for “FUNCTIONAL GROUNDIN9. Power (Indication label)10. Grounding reliability can only be achieved when this eq
“Hospital Only” or “Hospital Grade”.(For U.S.A., Canada
100-120VÅ`
220-240VÅ`
Japan/USA/Asia Console(100V)
(9)(10)
(7)
(2)
(1)
(3)
(4)
(5)
(6)
LOGI 52
Cons
formance to nationally recognized product safety roduct category, safety standard to which conformity
G
MOSEMAVOPOFR
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ole Labels (continued)
1.ETL Label: NRTL Listing and Certification Mark is used to designate constandards. The Mark bears the name and/or logo of the testing laboratory, pis assessed, and a control number.2.Identification and Rating Plate–USA/Asia 120V Console3.Identification and Rating Plate–Europe/Asia/USA 220V Console4.Identification and Rating Plate–Japan 120V Console
Figure 1-3. Label Location (b)
MADE FOR GE MEDICAL SYSTEMSMILWAUKEE, WISCONSIN BY
E YOKOGAWA MEDICAL SYSTEMS LTD. TOKYO, JAPAN
CLASS IDELRIALNUFACTUREDLTSWEREQUEMCY
LOGIQ 7
120Vac1200VA60Hz
1PHASE
GE Yokogawa Medical Systems
ETL LISTED
CONFORMS TOUL STD. 2601-1
46477
R
ETL TESTING LABORATORIES INC.CORTLAND, NEW YORK 13043
L I S TE D RL I S TE D
CERTIFIED TOCAN/CSA C22.2 NO. 601.1
C
~
(2) (4)(3)
(1)
LOGI 53
Fax B
You ca
286866-100, 101, 106, 127
291859-100, 101, 106, 127
291860-100
286865
orm Keene
Mailing Address
Direction Number
Attention:
Q 7 Quick Guide Direction 2291859-100 Rev. 1
ack Form
n order printed documentation by faxing this form to Coakley-Tech.
Basic User Manual 2
Quick Guide 2
Advanced Reference Manual 2
Basic Service Manual 2
Coakley-Tech (414) 389-9130 N
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