Technical Publications: Direction 5314626-100

GE
Healthcare
Technical Publications
Direction 5314626-100
Rev. 3
LOGIQ e User Guide
R5.2.x, R6.x.x
Operating Documentation
Copyright 2008 - 2010 By General Electric Co.
Regulatory Requirement
LOGIQ e complies with regulatory requirements of the following European

Directive 93/42/EEC concerning medical devices.
This manual is a reference for the LOGIQ e. It applies to all versions of the R5.2.x
and R6.x.x software for the LOGIQ e ultrasound system.
GE
Healthcare
GE Healthcare: 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
Revision History
Reason for Change
REV DATE (YYYY/MM/DD) REASON FOR CHANGE
Rev. 1 2008/09/17 Initial release
Rev. 2 2010/04/08 Update for software update and adding probes
Rev. 3 2010/11/29 Update to add Factory Site and CKD Rating Plate
List of Effected Pages

REVISION REVISION
PAGE NUMBER NUMBER PAGE NUMBER NUMBER
Title Page Rev. 3 Chapter 3 Rev. 3
Revision History Rev. 3 Chapter 4 Rev. 3
Regulatory Requirements Rev. 3 Chapter 5 Rev. 3
Table of Contents Rev. 3 Chapter 6 Rev. 3
Chapter 1 Rev. 3 Chapter 7 Rev. 3
Chapter 2 Rev. 3 Index Rev. 3
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop/ePDM (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 1 262 524 5698.
LOGIQ e User Guide i-1

Direction 5314626-100 Rev. 3
Regulatory Requirements
Conformance Standards
The following classifications are in accordance with the IEC/
EN 60601-1:6.8.1:
• According to 93/42/EEC Medical Device Directive, this is
Class IIa Medical Device.
• According to IEC/EN 60601-1,
• Equipment is Class I, Type B with BF or CF Applied Parts.
• Docking Cart console is Class I.
• According to CISPR 11,
• Equipment is Group 1, Class A ISM Equipment.
• Docking Cart is Group 1, Class A ISM Equipment.
• According to IEC 60529, the footswitch rate is IPx1
(FSU2001) or IPx8 (MKF 2-MED GP26, FSU-1000) .
This product complies with the regulatory requirement of the
following:
• Council Directive 93/42/EEC concerning medical devices:
the CE label affixed to the product testifies compliance to
the Directive.
The location of the CE marking is shown in the Safety
chapter of this manual.
Authorized EU Representative
European registered place of business:
GE Medical Systems Information Technologies GmbH
(GEMS IT GmbH)
Munzinger Strasse 5, D-79111 Freiburg, GERMANY
Tel: +49 761 45 43 -0; Fax: +49 761 45 43 -233
Conformance Standards (continued)
• International Electrotechnical Commission (IEC).
• IEC/EN 60601-1 Medical Electrical Equipment, Part 1
General Requirements for Safety.
i-2 LOGIQ e User Guide

• IEC/EN 60601-1-1 Safety requirements for medical
electrical systems.
• IEC/EN 60601-1-2 Electromagnetic compatibility -
Requirements and tests.
• IEC/EN 60601-1-4 Programmable electrical medical
systems.
• IEC/EN 60601-1-6 (Usability), EN 1041 (Information
supplied with medical devices).
• IEC 60601-2-37 Medical electrical equipment.
Particular requirements for the safety of ultrasonic
medical diagnostic and monitoring equipment.
• IEC 61157 Declaration of acoustic output parameters.
• International Organization of Standards (ISO)
• ISO 10993-1 Biological evaluation of medical devices.
• Underwriters’ Laboratories, Inc. (UL), an independent
testing laboratory.
• UL 60601-1 Medical Electrical Equipment, Part 1
• Canadian Standards Association (CSA).
• CSA 22.2, 601.1 Medical Electrical Equipment, Part 1
• NEMA/AIUM Acoustic Output Display Standard (NEMA
UD3).
• Medical Device Good Manufacturing Practice Manual
issued by the FDA (Food and Drug Administration,
Department of Health, USA).
Certifications
• General Electric Medical Systems is ISO 9001 and ISO
13485 certified.
Original Documentation
• The original document was written in English.
Country Specific Approval
• JAPAN
MHLW Certified Number: 218ABBZX00060000

Table of Contents
Conformance Standards - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2

Certifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-3
Original Documentation- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-3
Country Specific Approval - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-
4
Table of Contents Chapter 1 — Getting Started
Console Overview
Application Specific Systems - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-
2
Indications for Use - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3
Contraindication - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-
3 Prescription Device- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
1-3
Important Notices - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-4
Console graphics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6
Moving the System
Before moving the system - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-
17
When moving the system - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-17
System Start-Up
Power On - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-18
Power Off- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19
Probes
Connecting the Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-20
Cable Handling - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-22
Disconnecting the Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-22
Applications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-23
Features - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-24
Beginning an Exam
Scanning a New Patient - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-25
Patient Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-27
Chapter 2 — Performing an Exam
Optimizing the Image
B-Mode Controls- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2
M-Mode Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-4
Color Flow Mode Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-5
Doppler Mode Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-7

Other Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9
Measurement and Analysis
B-Mode Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12
Doppler Mode Measurements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18
M-Mode Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-22
Viewing and Editing Worksheets - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-24
Chapter 3 — After the Exam is Over
Probe Overview
Probe handling and infection control- - - - - - - - - - - - - - - - - - - - - - - - - - 3-2
Endocavitary Probe Handling Precautions- - - - - - - - - - - - - - - - - - - - - - 3-3
Probe Cleaning Process - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-4
Coupling gels - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-10
System Presets
Foreign Language Keyboard Setup - - - - - - - - - - - - - - - - - - - - - - - - - 3-11
Backup and Restore
Backup and restore strategy: patient data - - - - - - - - - - - - - - - - - - - - - 3-
16
Restore procedure: patient data- - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
Backup procedure: user-defined configurations - - - - - - - - - - - - - - - - - 3-18
Restore procedure: user-defined configurations- - - - - - - - - - - - - - - - - 3-19
Configuring Connectivity
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-
20 Connectivity Functions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
3-21
Electronic Documentation
Accessing Documentation Via a PC - - - - - - - - - - - - - - - - - - - - - - - - - 3-22
Using Online Help Via F1 - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-23
Contact Information
Contacting GE Healthcare Ultrasound - - - - - - - - - - - - - - - - - - - - - - - 3-24
Manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-28
Factory Sites - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-28
System Care and Maintenance
Inspecting the System- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-29
Weekly Maintenance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-30
Other Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33
Supplies/Accessories - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33
Chapter 4 — Safety
Safety Precautions
Precaution Levels- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
Hazard Symbols- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-3
Patient Safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5
Equipment and Personnel Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-8
Device Labels- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-14
EMC (Electromagnetic Compatibility) - - - - - - - - - - - - - - - - - - - - - - - - 4-19

Patient Environmental Devices- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-28
Acoustic Output - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-30
Warning Label Locations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-33
Chapter 5 — Emergency Department (ED)
Beginning an Exam
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2
Starting a New Patient- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
B-Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
M-Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Color Flow (CF) Mode- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7
Power Doppler Imaging (PDI) Mode - - - - - - - - - - - - - - - - - - - - - - - - - - 5-9
M Color Flow Mode- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-11
Pulsed Wave (PW) Doppler Mode - - - - - - - - - - - - - - - - - - - - - - - - - - 5-13
Chapter 6 — Nerve Block
Beginning an Exam
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2
Selecting an Application Preset and a Probe- - - - - - - - - - - - - - - - - - - - 6-4
B-Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-5
Chapter 7 — Using Touch Screen
Beginning an Exam
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-2
Touch Screen Display- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Selecting an Application Preset and a Probe- - - - - - - - - - - - - - - - - - - - 7-4
B-Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-5
M-Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-7
Measurement
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11
List of General Measurements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11
General Instructions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-12
Comment
General Instructions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13
Using CINE
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15

Activate CINE- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
CINE mode monitor display - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-16
Index

Chapter 1
Getting Started
Console Overview, Moving the System, System

Startup, Probes and Beginning an Exam
LOGIQ e User Guide 1-1

Getting Started
Console Overview
Application Specific Systems

For information on using the LOGIQ e system optimized for
Emergency Department use, refer to Chapter 5.
For information on using the LOGIQ e system optimized for
Nerve Block Guidance, refer to Chapter 6.
1-2 LOGIQ e User Guide

Console Overview
Indications for Use
The LOGIQ e is intended for use by a qualified physician for
ultrasound evaluation. Specific clinical applications and exam
types include:
• Fetal/Obstetrics
• Abdominal (including GYN)
• Pediatric
• Small Organ (including breast, testes, thyroid)
• Neonatal Cephalic
• Adult Cephalic
• Cardiac (adult and pediatric)
• Peripheral Vascular
• Intraoperative (abdominal, thoracic and peripheral)
• Thoracic/Pleural (fluid/motion detection)
• Musculo-skeletal Superficial
• Musculo-skeletal Conventional
• Urology (including prostate)
• Transrectal
• Transvaginal
• Transesophageal
CAUTION This machine should be used in compliance with law. Some

jurisdictions restrict certain uses, such as gender determination.
Contraindication
The LOGIQ e ultrasound system is not intended for ophthalmic
use or any use causing the acoustic beam to pass through the
eye.

Getting Started
Prescription Device
CAUTION: United States law restricts this device to sale or use
by, or on the order of a physician.
Important Notices
Do not attempt to install the system alone. General Electric,
Affiliate, or Distributor Field Engineers and Application
Specialists will install and setup the system. See ‘Contact
Information’ on page 3-24 for more information.
NOTICE This medical equipment is approved, in terms of the prevention
of radio wave interference, to be used in hospitals, clinics and
other institutions which are environmentally qualified. The use of
this equipment in an inappropriate environment may cause some
electronic interference to radios and televisions around the
equipment.
Ensure that the following is provided for the new system:
• A separate power outlet with a 6 amp circuit breaker for
220240 VAC or a 10 amp circuit breaker for 100-120
VAC.
• Take precautions to ensure that the console is
protected from electromagnetic interference.
Precautions include:
• Operate the console at least 15 feet away from motors,
typewriters, elevators, and other sources of strong
electromagnetic radiation.
• Operation in an enclosed area (wood, plaster or
concrete walls, floors and ceilings) helps prevent
electromagnetic interference.
• Special shielding may be required if the console is to
be operated in the vicinity of radio broadcast
equipment.
WARNING To avoid risk of fire, the system power must be supplied from a
separate, properly rated outlet.

Console Overview
Under no circumstances should the AC power plug be altered,
changed, or adapted to a configuration rated less than
specified. Never use an extension cord or adapter plug.
To help assure grounding reliability, connect to a “hospital
grade” or “hospital only” grounded power outlet.
Important Notices (continued)
Table 1-1: Example Plug and Outlet Configurations
AC DC Type Specification AC DC Type Specification
220-240 VAC, 2.5A 220-240 VAC, 2.5A

(China) (Switzerland)
220-240 VAC, 2.5A 220-240 VAC, 2.5A

(India) (U.K.)
220-240 VAC, 2.5A 100-120 VAC, 2.5A

(Argentina) (USA)
220-240 VAC, 2.5A 220-240 VAC, 2.5A

(Europe) (Israel)

Getting Started
100-120 VAC, 2.5A 220-240 VAC, 2.5A
(Japan) (Australia)
Console graphics
The following are illustrations of the console:
Figure 1-1. LOGIQ e System (opened view)
1. Handle
2. Soft Menu (use same as menu key)
3. LCD
4. Alphanumeric keys
5. Control Panel

Console Overview
Console graphics (continued)
Figure 1-2. LOGIQ e System (side views)
CAUTION Do not push objects into air vents and openings of LOGIQ e.
Doing so can cause fire or electric shock by shorting out interior
components.
CAUTION For compatibility reasons, use only GE approved probes,

peripherals or accessories.
DO NOT connect any probes or accessories without approval
by GE.
Battery
The lithium ion battery provides power when an AC power

source is not available. A battery in the battery bay is standard
with the LOGIQ e. Lithium ion batteries last longer than
conventional batteries and do not require replacement as often.

Getting Started
You can expect one hour of battery life while scanning with a
single fully charged battery.
The lithium ion technology used in your system’s battery is
significantly less hazardous to the environment than the lithium
metal technology used in some other batteries (such as watch
batteries). Used batteries should not be placed with common
household waste products. Contact local authorities for the
location of a chemical waste collection program nearest you.
NOTE: The battery is designed to work with LOGIQ e systems only.
Only use the batteries authorized by GE.
WARNING • The battery has a safety device. Do not disassemble or

alter the battery.
• Charge the batteries only when the ambient temperature is
between 0 and 40 degrees C (32 and 104 degrees F) and
discharge the batteries between 0 and 40 degrees C (32 and
104 degrees F).
• Do not short-circuit the battery by directly connecting the
negative terminals with metal objects.
• Do not heat the battery or discard it in a fire.
• Do not expose the battery to temperature over
50 degrees C (122 degrees F). Keep it away from fire and
other heat sources.
• Do not charge the battery near a heat source, such as a fire or
heater.
• Do not leave the battery in direct sunlight.
• Do not pierce the battery with a sharp object, hit it, or step on
it.
• Do not use a damaged battery.
• Do not solder a battery.
• Do not connect the battery to an electrical power outlet.

Console Overview
Battery (continued)
WARNING If the LOGIQ e is not being used on a monthly basis, the
battery needs to be removed during the lengthy non-use
period.
CAUTION To avoid the battery bursting, igniting, or fumes from the battery
causing equipment damage, observe the following
precautions:
• Do not immerse the battery in water or allow it to get
wet.
• Do not put the battery into a microwave oven or
pressurized container.
• If the battery leaks or emits an odor, remove it from all
possible flammable sources.
• If the battery emits an odor or heat, is deformed or
discolored, or in a way appears abnormal during use,
recharging or storage, immediately remove it and stop
using it. If you have any questions about the battery,
consult GE or your local representative.
• Short term (less than one month) storage of battery
pack:
• Store the battery in a temperature range between 0
degrees C (32 degrees F) and 50 degrees C (122
degrees F).
CAUTION • Long term (3 months or more) storage of battery pack:
• Store the battery in a temperature range between
-20 degrees C (-4 degrees F) and 45 degrees C
(113 degrees F)
• Upon receipt of the LOGIQ e and before first time
usage, it is highly recommended that the customer
performs one full discharge/charge cycle.

Getting Started
Battery (continued)
NOTE: A full discharge/charge cycle means the
system is turned on using battery power until the
battery loses its charge completely and the system
shuts down. Plug the LOGIQ e in until the battery is
fully charged as indicated by a green LCD light.
If the battery has not been used for >2 months, the
customer is recommended to perform one full
discharge/charge cycle. It is also recommended to
store the battery in a shady and cool area with FCC
(full current capacity).
• One Full Discharge/Charge Cycle Process:
1. Full discharge of battery to let the LOGIQ e
automatically shut down.
2. Charge the LOGIQ e to 100% FCC (full current
capacity).
3. Discharge of LOGIQ e for complete shut down
(takes one hour for discharge).
• When storing packs for more than 6 months, charge
the pack at least once during the 6 month timeframe to
prevent leakage and deterioration in performance.
• Use only GE recognized batteries.
View current When the system is running, there is a battery icon in the system
battery status status bar.
Figure 1-3. Battery icon
When you select this icon, the following appears:

Console Overview
Battery (continued)
Figure 1-4. Battery Status Message
Current power source–displays the current power source, AC

power or Battery.
Total battery power remaining–displays the current power
remaining capacity. When there is no battery, “Battery not
present” appears. When using a battery, it’s current capacity in
percent appears “current capacity (unit: percent)”. If the battery
is not in use, it states “current capacity (charging)”.
Warning information–displays warning information when
battery power is low. See Figure 1-5.
Battery power If the battery is in use and the battery power is low, a warning
low warning message appears to warn the user that the battery power is low
and that it needs to be charged.
Figure 1-5. Low battery power warning

Getting Started
Battery (continued)
NOTE: When the battery power is low and the user cannot charge the
battery in time, the system automatically shuts down in 2
minutes. This protects the whole system. You need to save all
unsaved data before the system shuts down or you may lose
useful information.
AC Adapter
CAUTION Do not use an AC adapter without approval by GE.
Be sure that nothing rests on the AC adapter’s power cable and
that the cable is not located where it can be tripped over or
stepped on.
Place the AC adapter in a ventilated area, such as a desk,
when you use it to run LOGIQ e. Do not cover the AC adapter
with paper or other items that will reduce cooling; do not use
the AC adapter inside a carrying case.
To prevent damage to the power cable of the AC adapter, DO
NOT pull excessively on the cable; DO NOT make any sharp
bends; DO NOT bend the power cable frequently.

Console Overview
Control Panel Map
Figure 1-6. Control Panel

1. Time Gain Compensation (TGC)
2. New Patient
3. Additional Feature Keys: Steer,
Harmonics, PDI
4. Mode/Gain/Auto keys: M-Mode,
Pulsed Wave
Doppler (PW)
Modes, Color Flow
(CF) Mode and B-
Mode
5. Imaging/Measurement Keys:
Cursor, Clear, Bodymark,
Measure, M/D Cursor,
Scan
Area, Set/B Pause
6. Depth/Zoom/Ellipse
7. Start/Stop (L/R)
8. Programmable Print Keys
9. Freeze
10. Keyboard

Getting Started
Top/Sub Menu
The Top/Sub Menu contains exam function and mode/function

specific controls.
NOTE: Different menus are displayed depending on which Top/Sub
Menu is selected.
Figure 1-7. Top/Sub Menu Controls
The Top/Sub Menu contains adjustable knobs associated with

it. The adjustable knobs are used to toggle optional functions
between up/down selections; the paddle switches are used to
access and adjust the menu. The functionality of these controls
change, depending upon the currently displayed menu.
The standard alpha-numeric keyboard has some special

Keyboard functions.
Esc Exit current display screen.
Help (F1 Key) Access Online help / user manual.
Arrow (F2 Key) Annotation arrow.
Eject (F3 Key) Eject media.
Spooler (F4 Key) Activates DICOM Job Spooler screen.
Reverse (F5 Key) Reverse.
User Defined Keys The following functions are available for the F6-F11 keys: TDI,
(F6 through F11 CWD, 3D, LOGIQ View, CrossXBeam, ECG On/Off, Set Home,
Keys) Text Overlay, Grab Last, Word Delete, Protocol and Video DVR.
Touch Screen Activates/deactivates Touch Screen Mode.
Mode On/Off (F12
Key)
Utility Enter the Utility function for system configuration and
customization.
Preset Access system Applications and presets.
Report Access the report page.

Direction 5314626-100 R
Console Over
Monitor Display
Figure 1-8. Monitor Display Tour
1. Institution/Hospital Name, Date, Time, Operator 13. Imaging Parameters by Mode.

Identification. 14. Focal Zone Indicator.
2. Patient Name, Patient Identification. 15. TGC.
3. Power Output Readout 16. Body Pattern.
4. GE Symbol: Probe Orientation Marker. 17. Depth Scale.
5. Image Preview. 18. Top/Sub Menu.
6. Gray/Color Bar. 19. Caps Lock (On or Off)
7. Cine Gauge. 20. Start Menu Icon
8. Measurement Summary Window. 21. Battery Icon
9. Image. 22. Card Icon
10. Measurement Calipers. 23. Trackball Functionality Status: Scroll, M&A
11. Measurement Results Window. (Measurement and Analysis), Position, Size,
12. Probe Identifier. Exam Preset. Scan Area Width and Tilt

Getting Started
Brightness
Adjusting the LCD monitor's brightness is one of the most

important factors for proper image quality.
The proper setup displays a complete gray scale. The lowest
level of black should just disappear into the background and
the highest white should be bright, but not saturated.
To adjust the brightness/volume:
1. On the alphanumeric keyboard,
• adjust brightness with the Ctrl + Up/Down keys;
• adjust volume with the Ctrl + Left/Right keys
Figure 1-9. Brightness and Volume
1. Brightness
2. Volume
NOTE: After readjusting the LCD monitor's Brightness, readjust all
preset and peripheral settings.
NOTE: The brightness of the LCD monitor should be set first as it
affects the Gain and Dynamic Range settings of your image.
Once set, this should not be changed unless the brightness of
your scanning environment changes.

Direction 5314626-100 R
Moving the System
Moving the System
Before moving the system

1. Shut down the system.See ‘Power Off’ on page 1-19 for
more information.
2. Unplug the power cord (if the system is plugged in).
3. Disconnect all cables from off-board peripheral devices
(external printer, etc.) from the console.
To prevent damage to the Power Cord, DO NOT pull
excessively on the cord or make sharp bends while
wrapping.
4. Store all probes in their original cases or in soft cloth or
foam to prevent damage.
5. Store sufficient gel and other essential accessories in the
special storage case.
When moving the system

1. Always use the handle to move the system.
CAUTION The system weighs approximately 4.6 kg (10.1 lbs). To avoid

possible injury and equipment damage:
• Do not let the system strike walls or door frame.
• Limit movement to a slow careful walk.

Getting Started
System Start-Up
Power On
CAUTION Press the Power On/Off switch to turn the power on. The
circuit breaker must also be in the on position.
Figure 1-10. LED Indicators
1. Indicates hard disk working status. When the LED is

flashing, the system is writing or reading from the hard disk.
Color: Green
2. Indicates power status. After pressing the Power On/Off
switch, the system power is on and this LED is lit. Color:
Green
3. Indicates battery status. When the battery is charged, the
LED is green. When battery power is low, the LED is
orange.
Color: Green and Orange
4. The fourth LED does not work on the LOGIQ e.
System Start-Up
Power Off
To power off the system:

1. When you shutdown the system, 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.

NOTE: DO NOT press and hold down the Power On/Off switch to
shutdown the system. Instead, lightly press the Power On/
Off switch and select Shutdown.
2. Using the Trackball, select Shutdown.
The shutdown process takes a few seconds and is
completed when the second LED turns from green to off.
NOTE: If the system has not fully shut down in 60 seconds, press
and hold down the On/Off switch until the system shuts
down.
3. Disconnect the probes.
Clean or disinfect all probes as necessary. Store them in
their shipping cases to avoid damage.
4. Disconnect AC adapter mains plug from the power outlet.
NOTE: Disconnect the AC adapter mains plug from the outlet to
ensure the system is disconnected from the power source.

Getting Started
Probes
Connecting the Probe

Probes can be connected at any time, regardless of whether the
console is powered on or off. To ensure that the ports are not
active, place the system in the image freeze condition.
To connect a probe:
1. Place the probe's carrying case on a stable surface and
open the case.
2. Carefully remove the probe and unwrap the probe cord.
3. DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage. Use the
integrated cable management hook to wrap the cord.
Inspect the probe before and after each use for damage or
degradation to the housing, strain relief, lens, seal and
connector. DO NOT use a transducer which appears
damaged until functional and safe performance is verified.
A thorough inspection should be conducted during the
cleaning process.
4. Align the connector with the probe port and carefully push
into place with the cable facing the front of the system.
5. Flip the connector locking lever up.
6. Carefully position the probe cord so it is free to move and is
not resting on the floor.
7. When the probe is connected, it is automatically activated.
Probes

Connecting the Probe (continued)
Figure 1-11. Probe connection to LOGIQ e
Figure 1-12. Probe connector locking handle
CAUTION Fault conditions can result in electric shock hazard. Do not

touch the surface of probe connectors which are exposed when
the probe is removed. Do not touch the patient when
connecting or disconnecting a probe.
Cable Handling
Take the following precautions with probe cables:
• Do not bend the cable acutely

Getting Started
Disconnecting the Probe
Probes can be disconnected at any time. However, the probe
should not be active when disconnecting the probe.
• Press the connector locking lever down.
• Pull the probe and connector straight out of the probe port.
• Carefully slide the probe and connector away from the
probe port and around the right side of the keyboard.
• Ensure the cable is free.
• Be sure that the probe head is clean before placing the
probe in its storage box or a wall hanging unit.

Probes
Applications
Table 1-2: Probe Indications for Use
Probe
Application
Abdomen X O X
Small Parts X O X X X O
Obstetrics X X
Gynecology X X
Pediatrics X O X O O O O X
Neonatal O X O O O
Urology X O
Cardiac X X X
Endocavity X
Transcranial O X
Intraoperative O O X O O O X X
Vascular O X O X X X X O
Biopsy O O O O O O

Getting Started
Transesophage X
al
Musculoskeletal X O X X X O
Conventional
Musculoskeletal X X
Superficial
Thoracic/ X X X
Pleural
X Main Application 0 Accessory Application
NOTE: 16L-RS is not available in China. *NOTE:

LOGIQ e R6.x.x only.
NOTE: 6Tc-RS probe can not be used with the Docking Cart.
Features
Table 1-3: Probe Features
Probe
Application
LOGIQ View X X X X X X X X X X X X
Virtual Convex X X X X X X
Virtual Apex X X X
Easy 3D X X X X X X X X X X
M Color Flow X X X X X X X X X X X X

Tru Access X X X X X X X X X X X X
Non-Imaging X X X X
CW
CrossXBeam X X X X X X X X X
ACO X X X X X X X X X X X X
Range Focus X X X X X X
TDI X X X
NOTE: 16L-RS is not available in China.

*NOTE: LOGIQ e R6.x.x only

Getting Started
Beginning an Exam
Scanning a New Patient

When starting a new patient’s exam, ensure you do the
following:
1. Press Patient.
2. Press New Patient on the Patient menu.
3. If there are images on the clipboard, a pop-up menu
appears. Specify whether you want to store images
permanently, delete images, or go to active images.
4. Choose the exam category.
5. Verify the dataflow.
NOTE: DO NOT use the removable media Data Flows on the New
Patient menu.
6. Fill in patient information.
NOTE: You can also select a patient from the patient database at
the bottom of the Patient menu if the patient has a patient
ID.
Columns drive the ordering of the patients displayed. The
column that you select drives the order of the displayed
patient database.
7. Select Register. Enter Past OB Exam information, if
desired.
Scanning a New Patient (continued)
8. Select the probe to start scanning (or select Exit, Esc,
Scan, or Freeze).
9. Perform the exam.
10. Store the raw data to the clipboard.
To store the still image, press Freeze and run the cineloop
using the Trackball. Select the frame and press P1 (or the
assigned Printer key).
To store the cineloop, press Freeze and run the cineloop
using the Trackball. Select the start/end frame and run the
selected loop. Press P1 (or the assigned Print key).
11. When you have completed the study, press End Exam.
The image management screen displays. Select the
LOGIQ e User Guide
Direction 5314626-100 Rev.
3
Beginning an Exam
images (still frame or cineloop) you want to store or select
Select All to store all images. Select Permanent Store to
store the images permanently.
1-26

Getting Started
Patient Screen
Figure 1-13. Patient Screen (Example: Category OB)
Enter Patient Data with the alphanumeric keyboard.

To navigate through the Patient Entry menu, use the Tab key or
Trackball and Set to move and fix the cursor.
The Patient Screen details are:
1. Image Management
• Patient–Provides a search and creation of patient.
(currently selected)
• Image History–Provides a list of images per exam for
the currently selected patient.
• Active Images–Provides preview of the currently
selected exam.
• Data Transfer–Provides an interface to handle patient
data from a remote device.
LOGIQ e User Guide

3
Beginning an Exam
Patient Screen (continued)

2. Function Selection
• New Patient–Used to clear patient entry screen in
order to input a new patient’s data into the database.
• Register–Used to enter new patient information into
the database prior to the exam.
NOTE: If you are using the auto-generate Patient ID feature, do not select
Register.
• Details–Select the Detail box to activate/deactivate the
exam details. Exam details include Indications,
Comments, Admission Number and Exam Description.
Figure 1-14. Detail Window
3. EZBackup–One-step method to backup patient images to

an external media.
EZMove–Move and delete patient images.
4. Dataflow Selection–Select the appropriate dataflow.
If you place the cursor on the icon, the pop-up menu
displays disk capacity.

Getting Started

WARNING Ensure you have selected a dataflow. If No Archive is selected,
no patient data is saved. A Ø appears next to Dataflow if No
Archive is selected.
5. Exit–Used to exit Patient Menu.

6. Patient Information
• Patient ID Number
• Other ID Number
The Other ID is used to add additional information of the
patient, such as Citizen ID.
NOTE: The Other ID field is only available on LOGIQ e R6.x.x.
NOTE: To enable/disable the Other ID field, go to Utility -->

Connectivity --> Miscellaneous.
NOTE: To select Other ID format, go to Utility --> Connectivity -
> Miscellaneous.
NOTE: The Other ID must be unique; The Other ID must be
accordant with the selected format.
• Patient Name–Last, First and Middle
• DOB (Birthdate)
• Age (automatically calculated when birthdate is input)
• Sex
7. Category Selection
Select from 8 exam application categories: Abdomen,
Obstetrics, Gynecology, Cardiology, Vascular, Urology,
Small Parts or Pediatrics.
When a category is selected, the measurement and
category presets are displayed.
8. Exam Information
Shows the Current/Active Exam information. Information
pertinent to the selected exam category appears in the
window. All possible information needs to be entered.
• Images–Displays the selected exam’s
images.
• Clear–Clears existing data.
• Past Exam (only for OB)–Input past exam
data (register the patient before using).
9. Patient View–Lists the patients in the database.

Beginning an Exam

• Search key–select search item from
Patient ID, Last Name, First Name,
Birthdate, Sex, Exam Date, Exam Today,
Accesstion Number, Exam Description,
Exam Date Before, Exam Date Between,
Exam Date After.
NOTE: If “Exam Date Between” is selected, the Input Dialog
displays and you can select the date from the displayed
calendar.
• String–enter appropriate information.
NOTE: In the Search String, the From and To dates are

separated by a “-” (dash) if “Exam Date Between” is
used for the Search key.
• Clear–Clears the entered string.
• Show All–Displays all patients in the database.
• Show XX/XX–Displays the searched (selected) patients

(number of patients currently displayed on the list/
number of patients in the database).
• Review–Select Patient/Exam for review.
• Resume Exam–Continues the exam for that patient if

you select the last exam of the day.
• New Exam–Creates a new exam on a current patient.
• Delete–Deletes Patient/Exam.
NOTE: “Delete” is only displayed when you login as

Administrator.
• Hide–Hides the Patient List Section.
• Lock/Unlock–Locks the exam/patient. Prevents move

and delete functions.
Exam View–Displays the Exam History of the selected
patient.
CAUTION To avoid patient identification errors, always verify the
identification with the patient. Make sure the correct patient
identification appears on all screens and hard copy prints.
CAUTION To maintain optimum performance and to safeguard patient
data, keep the total number of patients in the database below
1,000.

Getting Started

To reduce the total number of patients in the database, perform
the following procedure.
1. Prepare the unformatted CD-R, DVD-R or USB HDD before

EZBackup.
NOTE: Formatted CD-R or DVD-R cannot be used for EZBackup.
2. Backup all patient data by EZBackup. Before beginning
EZBackup, set the “Backup Files Older Than in Days” to “0”
on the Utility -> System -> Backup/Restore -> EZBackup/
Move screen to backup all data.
3. Go to the patient screen, select the patients/exams to
delete so the remaining number is less than 1,000. Select
“Delete” to delete the selected data.
NOTE: Removing image data with the “EZMove” function does not
reduce the patient number in the database.
NOTE: For each media to do EZBackup or Move, select a proper
capacity for the "Media capacity for estimate" preset under
Utility ->System ->Backup/Restore. For example, you can
select 700M for a CD or 4700M for a DVD.

Getting Started

Performing an Exam
Chapter 2
Performing an Exam
Optimizing the Image and Measurement and Analysis

B-Mode Controls
Table 2-1: B-Mode Controls

Possible
Bioeffect
Control Description/Benefit
Depth Yes Depth controls the distance over which the B-Mode images
anatomy. To visualize deeper structures, increase the depth. If there
is a large part of the display which is unused at the bottom, decrease
the depth.
Gain No B-Mode Gain increases or decreases the amount of echo

information displayed in an image. It may have the effect of
brightening or darkening the image if sufficient echo information is
generated.
Focus Yes Increases the number of focal zones or moves the focal zone(s) 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.
Auto Optimize No Auto lets you optimize the image based upon the actual B-Mode
image data (Auto Tissue Optimize, ATO). The preset levels (Low,
Medium, and High) allow you to pick a preference for the contrast
enhancement in the resulting image. Low does the least amount of
contrast enhancement, high does the most.
Auto is available in single or multi image, on live, frozen or CINE
images (in B-Mode only), and while in zoom, in Color Flow Mode,
and in Spectral Doppler.
Auto in Color Flow Mode automatically adjusts the overall color
gain.
Auto in PW Doppler Mode optimizes the spectral data. Auto adjusts
the Velocity Scale/PRF (live image only), baseline shift, dynamic
range, and invert (if preset). Upon deactivation, the spectrum is still
optimized.
The benefit of Auto can be found in reduced optimization time and a
more consistent and accurate optimization process.
M/D Cursor No Displays the Doppler Mode cursor on the B-Mode image.

Performing an Exam
Harmonics Yes Harmonics enhances near field resolution for improved small parts
imaging as well as far field penetration.
Frequency Yes Multi Frequency mode lets you downshift to the probe's next lower
frequency or shift up to a higher frequency.

Table 2-1: B-Mode Controls (Continued)
Possible
Bioeffect
CrossXBeam Yes CrossXBeam is the process of combining three or more frames from
different steering angles into a single frame.
The combined single image has the benefits of reduced speckle
noise, reduced clutter, and continuity of specular reflectors.
Therefore, this technique can improve contrast resolution with
increased conspicuity of low contrast lesions, better detection of
calcifications, biopsy needle visualization, and cystic boundary
definition.
TGC No
TGC amplifies returning signals to correct for the attenuation
caused by tissues at increasing depths. TGC slide pots are spaced
proportionately to the depth. The area each pot amplifies varies as
well. A TGC curve may appear on the display (if preset), matching
the controls that you have set (except during zoom). You can
choose to deactivate the TGC curve on the image.
Scan Area Yes You can widen or narrow the size of the sector angle to maximize
the image's region of interest (ROI).
Tilt Yes You can steer the sector angle to get more information without
moving the probe while in B-Mode, M-Mode, Doppler Mode, and
Color Flow Mode. Tilt is not available on Linear probes.
Angle Steer Yes You can steer the PW Doppler or Color Flow sector angle to get
more information without moving the probe.
Reverse No Flips the image 180 degrees left/right.
Dynamic Range No Dynamic Range controls how echo intensities are converted to
(Compression) shades of gray, thereby increasing the adjustable range of contrast.
The Dynamic Range control name changes to Compression on
frozen images.
Line Density Yes Optimizes B-Mode frame rate or spatial resolution for the best
possible image.
Map No The system supplies B, M, and Doppler Mode system maps.
Frame Average No Temporal filter that averages frames together, thereby using more
pixels to make up one image. This has the effect of presenting a
smoother, softer image.

Performing an Exam
Colorize No Colorize is the colorization of a conventional B-Mode image or
Doppler Spectrum to enhance the user's ability to discern B, M, and
Doppler Mode intensity valuations. Colorize is NOT a Doppler
Mode. Colorizes the gray scale image to enhance the eye’s
discrimination capability.
Spectrum Colorize colorizes the spectrum as a function of power
using the inverse of the Colorize map for the signal intensity in each
Doppler line. Colorize enhances the visibility of the spectrum's
characteristics and enhances your ability to identify spectral
broadening and the edge contours of the spectrum used to define
the peak frequency/velocity.
Table 2-1: B-Mode Controls (Continued)

Possible
Bioeffect
Edge Enhance No
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.
Rotation No
Flips the image 180 degrees up/down.
CAUTION: When reading an rotated image, be careful to observe
the probe orientation to avoid possible confusion over scan direction
or left/right image reversal.
Virtual Convex Yes On Linear probes, Virtual Convex provides a larger field of view in
the far field.
SRI HD No
SRI HD (Speckle Reduction Imaging High Definition) is an adaptive
algorithm to reduce the unwanted effects of speckle in the
ultrasound image.
B Softener No Affects the amount of lateral smoothing. It’s similar to dynamic

range by softening the appearance/edges of the image.
Virtual Apex Yes On sector probes, Virtual Apex provides a larger field of view in the
far field.
Range Focus Yes Improves the near/mid field image quality, borders/interfaces,
increases contrast and detail resolution across the image and
allows for less filling in the vessels.
CenterLine No The centerline of the image, for 12L-RS only.

B Steer+ Yes Slants the B-Mode or Color Flow linear image left/right to get more
information without moving the probe. The anglesteer function only
applies to linear probes.
Rejection No Selects a level below which echoes will not be amplified (an echo
must have a certain minimum amplitude before it will be
processed).
M-Mode Controls
Table 2-2: M-Mode Controls
Possible
Control Bioeffect Description/Benefit
Sweep Speed Yes Changes the speed at which the timeline is swept.
Available in M-Mode, Doppler Mode and M Color Flow Mode.
Anatomical M-Mode Yes Anatomical M-Mode gives you the ability to manipulate the cursor at
different angles and positions. The M-Mode display changes
according to the position of the cursor.
Color Flow Mode Controls
Table 2-3: Color Flow Mode Controls
Possible
Gain No Gain amplifies the overall strength of echoes processed in the Color
Flow window or spectral Doppler timeline.
Yes Increases/decreases the PRF on the color bar.

PRF (Pulse
Repetition
Frequency)
Wall Filter No Filters out low flow velocity signals. It helps get rid of motion artifacts
caused from breathing and other patient motion.
Color Scan Area Yes Scan Area sizes and positions the color window.

Performing an Exam
Invert (Color Invert) No Lets you view blood flow from a different perspective, e.g., red away
(negative velocities) and blue toward (positive velocities). You can
invert a real-time or frozen image.
NOTE: Invert reverses the color map, NOT the color PRF.
Baseline No Changes the Color Flow or Doppler spectrum baseline to

accommodate higher velocity blood flow. Minimizes aliasing by
displaying a greater range of forward flow with respect to reverse
flow, or vice versa.
Baseline adjusts the alias point. The default baseline is at the
midpoint of the color display and at the midpoint of the color bar
reference display.
Angle Steer Yes You can slant the ROI of the Color Flow linear image left or right to
get more information without moving the probe. The Angle Steer
function only applies to linear probes.
Color Flow Line Yes Optimizes the Color Flow frame rate or spatial resolution for the best
Density possible color image.
Map No Allows you to select a specific color map. After you have made your
selection, the color bar displays the resultant map.
Threshold No Threshold assigns the gray scale level at which color information
stops.
Frame Average No Averages color frames.
Transparency Map No Brings out the tissue behind the color map.
Spatial Filter No Smooths out the color, makes it look less pixely.
Table 2-3: Color Flow Mode Controls (Continued)

Possible
Bioeffect
Packet Size Yes Controls the number of samples gathered for a single color flow
vector.

Power Doppler No Power Doppler Imaging (PDI) is a color flow mapping technique
Imaging (PDI) used to map the strength of the Doppler signal coming from the
tissue rather than the frequency shift of the signal. Using this
technique, the ultrasound system plots color flow based on the
number of reflectors that are moving, regardless of their velocity.
PDI does not map velocity, therefore it is not subject to aliasing.
M Color Flow Mode Yes M Color Flow is used for fetal cardiac applications. Color Flow
overlays color on the M-Mode image using velocity and variance
color maps. The Color Flow wedge overlays the B-Mode image and
M-Mode timeline.
The Color Flow maps available in M-Mode are the same as in Color
Flow Mode. The size and position of the Color Flow window in
BMode determines the size and position of the Color Flow window
in M-Mode.
All M-Mode measurements are available with M Color Flow active:
depth, distance along a straight line, % stenosis, volume, trace,
circumference, enclosed area, distance, time, slope, and heart rate.

Performing an Exam
Doppler Mode Controls
Table 2-4: Doppler Mode Controls
Possible
B Pause Yes Toggles between simultaneous and update presentation while

viewing the timeline.
Yes
Doppler sample Moves the sample volume gate on the B-Mode's Doppler Mode
volume gate position cursor. The gate is positioned over a specific position within the
(Trackball) vessel.
Doppler sample Yes Sizes the sample volume gate.

volume length
PRF Yes Adjusts the velocity scale to accommodate faster/slower blood

flow velocities. 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.
Angle Correct No Estimates the flow velocity in a direction at an angle to the Doppler
vector by computing the angle between the Doppler vector and the
flow to be measured.
NOTE: When the Doppler Mode Cursor and angle correct indicator
are aligned (the angle is O), you cannot see the angle correct
indicator.
Quick Angle No Quickly adjusts the angle by 60 degrees.
Wall Filter No Insulates the Doppler signal from excessive noise caused from
vessel movement.
Baseline No Adjusts the baseline to accommodate faster or slower blood flows to

eliminate aliasing.
M/D Cursor No Displays the Doppler Mode cursor on the B-Mode image.
Audio Volume No Controls audio output.

Invert No Vertically inverts the spectral trace without affecting the baseline
position.
Dynamic Range No Dynamic range controls how echo intensities are converted to
shades of gray, thereby increasing the range of contrast you can
adjust.
Spectral Trace No Traces the average mean and peak velocities in realtime or frozen
(Trace Method) images.
Trace Sensitivity No Adjust the trace to follow the waveform for signal strength.
Cycles to Average No The average value over a number of cycles (from 1-5).
Trace Direction No Specifies trace direction.
Table 2-4: Doppler Mode Controls (Continued)

Possible
Bioeffect
Full Timeline No Expands display to full timeline display.
Display Format No Changes the horizontal/vertical layout between B-Mode and

MMode, or timeline only.
Duplex/Triplex No
Duplex allows two modes to be active at the same time (B+PW or
B+CW or B+CF); Triplex allows three modes to be active at the
same time (C+PW+CF or B+CW+CF).
When Duplex/Triplex is OFF, either the image or timeline is active.
B Pause then switches the activce side between image and the
timeline.
With Duplex/Triplex active, M/D Cursor functions the same as the
Duplex/Triplex control by cycling Duplex/Triplex on/off. B-Pause
pauses the image while keeping the CW / PW timeline active.
Time Resolution No Adjusts image appearance so that if you select a lower setting, the
image appears smoother; if you select a higher setting, the image
appears sharper.
Spectral Average No Averages the spectrum in a vertical direction and timeline direction.
Modify Auto Calcs No Activates the menu to select which calculations are automatically
calculated.

Performing an Exam
Auto Calcs No Activates the calculation automatically which you select in the
Modify Auto Calculation when the system is in a state of freeze or
live.
Continuous Wave No Allows examination of blood flow data all along the Doppler Mode
Doppler (CWD) cursor rather than from any specific depth. Gather samples along
the entire Doppler beam for rapid scanning of the heart. Range
gated CW allows information to be gathered at higher velocities.
Other Controls
Zoom
Zoom is used to magnify a zoom region of interest (ROI). The

system adjusts all imaging parameters accordingly. You can also
zoom frozen images.
Acoustic Observe the output display for possible effects.

Output
Hazard
To zoom an image, adjust Zoom. A reference image appears in

the upper, left-hand section of the display.
To exit zoom, adjust Zoom until the reference zoom image is
removed or press B-Mode.
Freezing an image
To freeze an image,
1. Press Freeze. The key backlights.
If you are in a mixed mode, both screen formats stop
immediately. Deactivating Freeze restarts both modes and
places a black bar on the trace to indicate the time discontinuity.
To reactivate the image,
1. Press Freeze again.
NOTE: Deactivating Freeze erases all measurements and calculations
from the display (but not from the worksheet).
Use the Trackball to start CINE after pressing Freeze.
Activating CINE
To activate CINE,

1. Press Freeze.
2. Move the Trackball.
Body Patterns
To activate body patterns, press the Body Mark control.

Select the desired body pattern with the Top/Sub Menu
controls. The selected body pattern is displayed on the
monitor.
Press the Move Pattern control on the Top/Sub Menu to
reposition the body pattern with the Trackball and Set controls.
A probe mark is associated with the body patterns and illustrates
the probe position on the body pattern. This marker can be
placed with the Trackball and rotated with the Rotate Pattern
control.
The probe mark type is selectable by rotating the Probe Type
control on the Top/Sub Menu. There are different choices
available with one being a blank selection.
To select the active side in dual B-Mode, use the Active Side
rotary control at the bottom of the Top/Sub Menu.
Press Clear to erase the body pattern. The pattern is erased
and the system exits the body pattern mode.

Performing an Exam
Annotating an Image
Pressing the Comment key or any keys on the alphanumeric

keyboard initiates the comment mode. This assigns the trackball
function to controlling the cursor and displays the comment
library on the Top/Sub Menu menu.
In comment mode, text can be added by using the comment
library or by typing from the alphanumeric keyboard.
After activating the comment mode, a vertical bar type cursor
appears on the screen. Use the Trackball to move the cursor.
To delete all comments, press the Clear key twice immediately
after entering the comment mode.
Arrow pointers can be used by activating the F2 (Arrow) key on
the keyboard. When the pointer comes up, it is a GREEN color,
indicating it is active and can be moved.

B-Mode Measurements
Two basic measurements can be made in B-Mode.
• Distance
• Circumference and Area
• Ellipse Method
• Trace Method
• Spline Method
NOTE: The following instructions assume that you first scan the
patient and then press Freeze.

Performing an Exam
Distance measurement
To make a distance measurement:

1. Press Measure once; an active caliper 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 active caliper at the end point, move
the Trackball.
A dotted line connects the measurement points, if preset
accordingly.
5. To complete the measurement, press Set.
The system displays the distance value in the Results
Window.
The following hints can help you to perform distance
measurements:
HINTS • Before you complete a measurement:

• To toggle between active calipers, press Measure.
• To erase the second caliper and the current data measured
and start the measurement again, press Clear once.
• After you complete the measurement:
• To rotate through and activate previously fixed calipers,
adjust Cursor Select.
• To erase all data that has been measured to this point, but
not data entered onto worksheets, press Clear.
Circumference and area (ellipse) measurement
You can use an ellipse to measure circumference and area. To

measure with an ellipse:
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. Adjust the Ellipse control; an ellipse with an initial circle
shape displays.
6. To position the ellipse and to size the measured axes
(move the calipers), move the Trackball.
7. To increase the size, adjust the Ellipse control in a
clockwise direction. To decrease the size, adjust 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 Results
Window.
HINTS Before you complete the ellipse 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.
Circumference and area (trace) measurement
Trace To trace the circumference of a portion of the anatomy and
calculate its area:
1. Press Measure until 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.
displays the circumference and the area in the Results
Window.

Performing an Exam
Open Trace To trace the circumference of a portion of the anatomy and
calculate its length:
NOTE: For open trace, Area (A) is not displayed in the result
window.
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.
displays the circumference and the length in the Results
Window.
HINTS Before you complete the trace measurement:

• To erase the line (bit by bit) back from its current point,
move the Trackball or adjust 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.
Circumference and area (spline trace) measurement
To trace the circumference of a portion of the anatomy and

calculate its area:
2. To position the first caliper at the start point, move the
Trackball.
3. To fix the trace start point, press Set. The first caliper turns
yellow. The second caliper appears at the same position as
the first caliper and is green.
NOTE: When pressing the Clear key once, the second caliper
disappears and the first caliper is activated.

If Clear is pressed again, the first caliper disappears and
the Spline trace is cancelled.
4. To position the second caliper, move the Trackball 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.
5. 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. To enable spline trace, modify the
Measure Key Sequence preset found in Utility -> Measure >
Advanced preset menu.
Circumference and area (spline trace) measurement (continued)
Edit the 1. Select Cursor Select. The spline trace changes to green
spline trace and all points appear on the trace as yellow.
A pick-caliper appears on the center of the image and the
message “Edit spline trace” displays at the bottom of the
screen.
NOTE: The pick-caliper is used to select and move the trace points.
Figure 2-1. Edit spline trace
Select Cursor Select again. The trace is deactivated

(changes to yellow) and all points, including the pick-caliper,
are removed.
If the previous/next fixed caliper exists on the image, it is
activated.

Performing an Exam
NOTE: Pressing Clear at this time removes all points and the trace
graphic.
2. Move the pick-caliper to the desired point and press Set.
The point is activated and turns green.
3. Move the point to the desired position and press Set. The
point is fixed and turns yellow. The pick-caliper appears on
the center of the image.
NOTE: The spline trace is updated at run time.
NOTE: To remove a point, press Clear while moving the point. The
trace turns green and the remaining points continue to be
shown as yellow. If there are less than three points, the
spline trace is removed.
4. Press Set again. All points are removed from the trace and
the trace is shown as yellow.
Doppler Mode Measurements
Four basic measurements can be made in Doppler Mode.
• Velocity
• TAMAX and TAMEAN (Manual or Auto Trace)
• Two Velocities with the Time Interval and Acceleration
between them
• Time Interval
NOTE: The following instructions assume that you do the following:
1. In the B-Mode part of the display, scan the anatomy you
want to measure.
2. Go to the Doppler Mode part of the display.
3. Press Freeze.
Velocity
To measure velocity:
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.

displays the velocity measurement in the Results Window.
TAMAX and TAMEAN
Manual Trace The value measured depends upon the Vol Flow Method preset.
The two selections available are: Peak (TAMAX) and Mean
(TAMEAN).
To do a manual trace of TAMAX or TAMEAN:
1. Press Measure twice; a trace caliper displays.
2. To position the caliper at the trace start point, move the
Trackball.
4. To trace the maximum values of the desired portion of the
spectrum, move the Trackball.
NOTE: To edit the trace line, move the Trackball.
displays the measurement values in the Results Window.
Auto Trace The value measured depends upon the Vol Flow Method preset.
The selection available is the Peak (TAMAX).
To auto trace TAMAX:
1. Press Measure twice; an active caliper with a vertical
dotted line displays.
2. To position the caliper at the trace start point in the Doppler
spectrum, move the Trackball.
4. To position the vertical caliper at the end point, move the
Trackball.
automatically fixes both calipers and traces the maximum
value between the two points. The system displays this
value in the Results Window.
NOTE: When you set the Auto Trace for Both (above and below),
the system picks up the maximum power of the signal, NOT
the maximum velocity. If the maximum velocity is not the
maximum power, the system may not trace accurately. If
you want to use maximum velocity, select either Above or
Below.

Performing an Exam
Edit Trace Auto Trace can be edited after taking an Auto Trace
measurement.
1. After taking an Auto Trace measurement, select the
measurement result on the result window. The Edit Trace
(Edit Peak or Edit Mean) menu window appears.
NOTE: If the system cannot take the trace data correctly from the
image, Edit Trace does not work.
2. Select Edit Trace. The first caliper (manual trace caliper)
appears on the center of the image. Use the Trackball to
move the caliper on the trace line to the start point.
NOTE: To cancel Edit Trace at this time, press Clear or Freeze.
3. Press Set to fix the first caliper. The second caliper appears.
Edit the trace manually using the second caliper.
The Ellipse control is used to edit the trace.
NOTE: When pressing the Clear key once at this time, the second
caliper disappears and the first caliper appears in the center
of the image.
NOTE: If you press Freeze at this time, the caliper is automatically
fixed and the result window updates.
4. Press Set to fix the second caliper. The trace and the result
window update. The trace data (TAMAX and TAMEAN) are
updated, though the other points (e.g. PS, ED) are not
updated by trace. The points can be edited with Cursor
Select.
NOTE: While in Edit Trace, Cursor Select is disabled.
5. Repeat Edit Trace as needed.
Velocity, Time Interval and Acceleration
To measure two velocity values, the time interval (ms), and

acceleration (m/s2):
1. Press Measure three times; an active caliper with vertical
and horizontal dotted lines displays.
2. To position the caliper at the start point, move the
Trackball.

4. To position the second caliper at the end point, move the
Trackball.
displays the two peak end point velocities, the time interval,
and the acceleration in the Results Window.
Time interval
To measure a horizontal time interval:

1. Press Measure four times; an active caliper with a vertical
Trackball.
Trackball.
displays the time interval between the two calipers in the
Results Window.
M-Mode Measurements
Basic measurements that can be taken in the M-Mode portion
of the display are:
• Tissue Depth (Distance)
• Time Interval
• Time Interval and Velocity
NOTE: The following instructions assume that you do the following:
1. In the B-Mode part of the display, scan the anatomy you
want to measure.
2. Go to the M-Mode part of the display.
3. Press Freeze.
Tissue depth
Tissue depth measurement in M-Mode functions the same as
distance measurement in B-Mode. It measures the vertical
distance between calipers.

Performing an Exam
1. Press Measure once; an active caliper with a vertical and
horizontal dotted line displays.
2. To position the active caliper at the most anterior point you
want to measure, move the Trackball.
active caliper.
4. To position the second caliper at the most posterior point
you want to measure, move the Trackball.
The system displays the vertical distance between the two
points in the Results Window.
Time interval
To measure a horizontal time interval and velocity:

1. Press Measure twice; an active caliper with a vertical
2. To position the caliper at the start point, move the
Trackball.
3. To fix the first caliper, press Set. The system fixes the first
Trackball.
displays the time interval between the two calipers in the
Results Window.
Time interval and Velocity
To measure time and velocity between two points:

1. Press Measure three times; an active caliper with a vertical
and horizontal dotted line displays.
Trackball.

active caliper.
Trackball.
The system displays time(s) and slope between the two
points in the Results Window.
Viewing and Editing Worksheets
NOTE: Worksheets are not saved if the system crashes.
As you complete measurements, the system puts measurement
data in the appropriate worksheets.
To view a worksheet
To view a worksheet, select Worksheet on the Top/Sub Menu.

The system displays the worksheet for the current study.
To view a different worksheet, select the worksheet key for the
desired worksheet.

Performing an Exam
Figure 2-2. OB B-Mode Worksheet
To return to scanning, do one of the following:

• Select Worksheet.
• Press Esc.
To view a worksheet (continued)
To view worksheet data for a particular mode, select the key for
that mode. To view a worksheet with data for more than one
mode, select Expand. When Expand is selected, it defaults to
view all measurements, noted by mode, on the worksheet.
If a worksheet has more data on a second page, to view the
next page, adjust the Page Change control.

To edit a worksheet
To change data on a worksheet:

1. To position the cursor at the field you want to change, move
the Trackball. The field is highlighted.
2. Press Set.
3. Type the new data in the field. The new data is displayed in
blue to indicate that it was manually entered.
To delete or exclude data on a worksheet:
1. To position the cursor at the field you want to delete or
exclude, move the Trackball. The field is highlighted.
2. Do one of the following:
• To delete the field, select Delete Value.
• To exclude the field, select Exclude Value.
The data in the field is not visible and is not included in
worksheet calculations.
• To include a value that you previously excluded, select
Exclude Value.
To type a comment on a worksheet:
1. Select Comments. The Comments window opens.
2. Type comments about the exam.
3. To close the Comments window, select Comments.
HINTS Some fields on the worksheet are view only, and others you can
change or select. To easily see which fields you can change or
select, move the Trackball. As the cursor moves over a field
that you can change or select, the field is highlighted.

Chapter 3
After the Exam is Over
Probe Overview, System Presets, DataBackup,

Configuring Connectivity, Electronic Documentation and

Probe Overview
Probe handling and infection control

This information is intended to increase user awareness of the
risks of disease transmission associated with using this
equipment and provide guidance in making decisions directly
affecting the safety of the patient as well as the equipment user.
Diagnostic ultrasound systems utilize ultrasound energy that
must be coupled to the patient by direct physical contact.
Depending on the type of examination, this contact occurs with
a variety of tissues ranging from intact skin in a routine exam to
recirculating blood in a surgical procedure. The level of risk of
infection varies greatly with the type of contact.
One of the most effective ways to prevent transmission between
patients is with single use or disposable devices. However,
ultrasound transducers are complex and expensive devices that
must be reused between patients. It is very important, therefore,
to minimize the risk of disease transmission by using barriers
and through proper processing between patients.
CAUTION Risk of Infection. ALWAYS clean and disinfect the probe

between patients to the level appropriate for the type of
examination and use FDA-cleared probe sheaths where
appropriate. See ‘Supplies/Accessories’ on page 3-33 for
ordering information.
CAUTION 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 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

Probe Overview
chemical sterilants because of the possibility of neuro toxic
residues remaining on the probe.
Endocavitary Probe Handling Precautions
If the sterilization solution comes out of the endocavitary probe,
please follow the cautions below.
CAUTION Sterile/sanitary sheaths are to be used on the probe during its

actual use with patients. Wearing gloves protects the patient
and operator.
CAUTION Sterilant Exposure to Patient (e.g., Cidex)—Contact with a

sterilant to the patient’s skin or mucous membrane may cause
an inflammation. If this happens, refer to the sterilant’s
instruction manual.
Sterilant Exposure from Probe Handle to Patient (e.g.,
Cidex)—DO NOT allow the sterilant to contact the patient. Only
immerse the probe to its specified level. Ensure that no solution
has entered the probe’s handle before scanning the patient. If
sterilant comes into contact with the patient, refer the the
sterilant’s instruction manual.
Sterilant Exposure from Probe Connector to Patient (e.g.,
Cidex)—DO NOT allow the sterilant to contact the patient. Only
immerse the probe to its specified level. Ensure that no solution
has entered the probe’s connector before scanning the patient.
If sterilant comes into contact with the patient, refer the the
sterilant’s instruction manual.
Endocavitary Probe Point of Contact—Refer to the sterilant’s
instruction manual.

Probe Cleaning Process
Cleaning probes
Perform After To clean the probe:
Each Use
1. Disconnect the probe from the ultrasound console and
remove all coupling gel from the probe by wiping with a soft
cloth and rinsing with flowing water.
2. Wash the probe with mild soap in lukewarm water. Scrub
the probe as needed using a soft sponge, gauze, or cloth to
remove all visible residue from the probe surface.
Prolonged soaking or scrubbing with a soft bristle brush
(such as a toothbrush) may be necessary if material has
dried onto the probe surface.
CAUTION Take extra care when handling the lens face of the
Ultrasound transducer. The lens face is especially sensitive
and can easily be damaged by rough handling. NEVER use
excessive force when cleaning the lens face.
3. Rinse the probe with enough clean potable water to

remove all visible soap residue.
4. Air dry or dry with a soft cloth.
Cleaning probes (continued)
Figure 3-1. Probe Immersion Levels

Probe Overview
1. Fluid Level
2. Aperature
3. Contact face within Patient Environment
Disinfecting probes
Perform After Ultrasound probes can be disinfected using liquid chemical

Each Use germicides. The level of disinfection is directly related to the
duration of contact with the germicide. Increased contact time
produces a higher level of disinfection.
Table 3-1: Description of Pictogram on Care card
Pictogram Description
“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.
Biohazard - Patient/user infection due to contaminated equipment.

Usage
• Cleaning and care instructions
• Sheath and glove guidelines
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 use.
Do not immerse the probe into any liquid beyond the level specified for that
probe. Refer to the user manual of the ultrasound system.

Since there is a possibility of having negative effects on the probe, observe the
specified immersing time by the germicide manufacturer strictly. Do not
immerse the probe in liquid chemical germicides more than the time prescribed
in the care card.

Probe Overview
Disinfecting probes (continued)
CAUTION Review the probe care card that is packed with each probe. The
following website contains the most current and up-to-date
recommendations:
http://www.gehealthcare.com/usen/ultrasound/products/
probe_care.html
Cidex Plus has been approved for all probes available on the
LOGIQ e.
Pera Safe high level disinfectant has been approved for the
E8C-RS, 8C-RS and 12L-RS probes.
T-spray low-level disinfectant has been approved for the
E8CRS, 8C-RS, 12L-RS, 3S-RS and 8L-RS probes. T-Spray II
has been approved for all the probes available on the LOGIQ e
except 6Tc-RS.

CAUTION 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.
You MUST disconnect the probe from the LOGIQ e prior to
cleaning/disinfecting the probe. Failure to do so could damage
the system.
DO NOT soak probes in liquid chemical germicide for longer
than is stated by the germicide instructions for use. Extended
soaking may cause probe damage and early failure of the
enclosure, resulting in possible electric shock hazard.
1. Prepare the germicide solution according to the

manufacturer's instructions. Be sure to follow all precautions
for storage, use and disposal.
2. Place the cleaned and dried probe in contact with the
germicide for the time specified by the germicide
manufacturer. High-level disinfection is recommended for
surface probes and is required for endocavitary and
intraoperative probes (follow the germicide manufacturer's
recommended time).
CAUTION Probes for neuro surgical intra-operative use must NOT be

sterilized with liquid chemical sterilants because of the
possibility of neuro toxic residues remaining on the probe.
Neurological procedures must be done with the use of
legally marketed, sterile, pyrogen free probe sheaths.
3. After removing from the germicide, rinse the probe following

the germicide manufacturer's rinsing instructions. Flush all
visible germicide residue from the probe and allow to air dry.

Probe Overview
WARNING CREUTZFIELD-JAKOB DISEASE

Failure of the probe sheath or direct contact of the probe with
dura or any intra-cranial tissue of patients with CreutzfieldJakob
disease requires that the probe be destroyed. There is no
effective means for decontamination of the probe. For more
information, see the Center of Disease Control and Prevention
http://www.cdc.gov/ncidod/hip/sterile/cjd.htm.
Biological
Hazard
WARNING 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.

System Presets
Coupling gels
WARNING Do not use unrecommended gels (lubricants). They may

damage the probe and void the warranty.
Applying In order to assure optimal transmission of energy between the

patient and probe, a conductive gel or couplant must be applied
liberally to the patient where scanning will be performed.
CAUTION Do not apply gel to the eyes. If there is gel contact to the eye,
flush eye thoroughly with water.
Precautions Coupling gels should not contain the following ingredients as

they are known to cause probe damage:
• Methanol, ethanol, isopropanol, or any other alcohol-based
product
• Mineral oil
• Iodine
• Lotions
• Lanolin
• Aloe Vera
• Olive Oil
• Methyl or Ethyl Parabens (para hydroxybenzoic acid)
• Dimethylsilicone
• Polyether glycol based

System Presets
Foreign Language Keyboard Setup
Keyboard Setup for non-Russian/Greek/Chinese/Japanese Languages
To set up the keyboard for non-Russian/Greek/Chinese/

Japanese languages:
NOTE: You must apply the changes on each setup page before moving to
the next page.
1. In Utility--> System--> General, set the Language as desired. Save
this setting.
2. Press Regional Options, select the Language tab, press
Details, under Installed Services press Add to set the
Keyboard layout/IME to United States-International, press
OK, set the Default input language to English (United
States) - United States International, press Apply, Press OK.
Figure 3-2. Selecting the International Keyboard

System Presets
Keyboard Setup for non-Russian/Greek/Chinese/Japanese Languages
(continued)
3. Select the Advanced tab, then select the language in the

Language for non-Unicode programs pull-down menu.
Press Apply. Answer Yes to use files already loaded on the
hard disk, then answer No to not reboot the system yet,
press OK. Press Save and Exit the Utility screen.
Figure 3-3. Set Language
4. Reboot the system. When your system restarts, the system

appears in the selected language.
5. To type foreign characters, press Ctrl+Shift to change the
keyboard to the international keyboard.
Keyboard Setup Procedure for Russian/Greek/Chinese/Japanese
1. In Utility--> System--> General, set the Language as

Russian/Greek/Chinese/Japanese. Save this setting.

Figure 3-4. Changing the System Language to Russian/Greek/

Chinese/Japanese
2. Press Regional Options, under Standards and Formats

select Russian, Greek, Jpanese or Chinese (PRC). Under
Location select Russia, Greece, Japan or China. Press
Apply.
Figure 3-5. Regional Options
3. Select the Language tab, press Details, under Installed

Services select the Russian, Greek, Japanese or Chinese
(PRC) keyboard, under Default input language select
Russian - Russian, Greek - Greek, Japanese - Japanese or
Chinese (PRC) - Microsoft IME 3.0. Press Apply, Press OK.
(continued)
4. Select the Advanced tab, then select Russian, Greek,

System Presets
Japanese or Chinese (PRC) in the Language for
nonUnicode programs pull-down menu. Press Apply.
Answer Yes to use files already loaded on the hard disk,
then answer No to not reboot the system yet, press OK.
Press Save and Exit the Utility screen.
Figure 3-6. Set Language
5. Reboot the system. When your system restarts, the system

appears in the selected language.
6. To switch between the English and Russian (or Greek or
Japanese or Chinese) keyboard, press Ctrl+Shift to change
the keyboard to the Russian, Greek or Chinese keyboard.
7. Apply the changes by pressing Apply. Press OK TWICE.
NOTE: To have the settings take effect, you MUST turn off the system
and turn it back on.
(continued)
Here is an example of the Russian keyboard:

Figure 3-7. Russian Keyboard

System Presets
Backup and Restore
Backup and restore strategy: patient data

To minimize accidental loss of data, perform backup of the
patient archives stored on the local hard drive DAILY as
described in this section. Use a Backup/Restore disk to back up
patient archives from the hard drive, using the backup procedure
described in this section. Data from the Backup/Restore disk
may be restored to the local hard drive using the restore
procedure.
CAUTION The restore procedure overwrites the existing database on the

local hard drive.
CAUTION Make sure to verify the media after writing of data, such as
EZBackup, SaveAs or Export.
Before deleting a patient or image from the patient screen,
make sure you have saved the data by EZBackup/Backup or
Export and verify that the media transfer of data was
successful.
NOTE: To perform backup and restore procedures, you must login with
administrator privileges.

Backup and Restore
Restore procedure: patient data

local hard drive. Make sure to insert the correct media.
You cannot restore the data between systems with different
software versions.
1. Insert the media into the media drive.

2. On the Control Panel, press Utility.
3. Select System.
4. On the monitor display, select Backup/Restore. The
Backup/Restore screen is displayed.
NOTE: If you are not logged in with administrator privileges, the
Operator Login window is displayed. Log on with
5. In the Restore list, select Patient Archive.
6. In the Media field, select the Backup/Restore media.
7. Select Restore.
The system performs the restore. As it proceeds, status
information is displayed on the Backup/Restore screen.
Backup procedure: user-defined configurations
CAUTION To avoid the risk of overwriting the local patient archives on the
system to update, DO NOT check Patient Archive when making
a backup of configuration settings.
1. Insert media into the media drive.

3. Select System.
4. On the monitor display, select
Backup/Restore.
The Backup/Restore screen is displayed.
LOGIQ e User Guide

3
5. In the Backup list, select User Defined
Configuration.
6. In the Media field, select a media.
7. Select Backup.
The system performs the backup. As it proceeds, status
information is displayed on the Backup/Restore screen.
8. After the backup is complete, press F3
to eject the media. 3-18

Backup and Restore
Restore procedure: user-defined configurations

local hard drive. Make sure to insert the correct media.
DO NOT restore data between systems with different software
versions.
CAUTION To avoid the risk of overwriting the local patient archives, DO

NOT check Patient Archive when restoring user-defined
configurations.
1. Insert the media with the user-defined configurations into

the drive.
3. Select System.
4. On the monitor display, select Backup/Restore.
The Backup/Restore screen is displayed.
5. In the Restore list, select from the following, depending on
which configurations you want to restore:
• User Defined Configuration
Select the parameters to be restored in the Detailed
Restore section.
• Imaging Presets
• Connectivity Configuration
• Measurement Configuration
• Comment/Body Pattern Configuration
• All Others
6. In the Media field, select the media.
7. Select Restore.
The system performs the restore. As it proceeds, status
information is displayed on the System/Backup/Restore
screen. The system restarts.
LOGIQ e User Guide

3
Overview
You use Connectivity functionality to set up the connection and
communication protocols for the ultrasound system. This page
gives an overview of each of the Connectivity functions. Each
function is described in detail in the following pages.

Connectivity Functions
To set up your institution’s connectivity, you must login with
1. TCPIP: allows you to configure the Internet Protocol.
2. Device. allows you to set up devices.
3. Service: allows you to configure a service (for example,
DICOM services such as printers, worklist, and other
services such as video print and standard print) from the list
of supported services. This means that the user can
configure a device with the DICOM service(s) that particular
device supports.
4. Dataflow: allows you to adjust the settings of the selected
dataflow and associated services. Selecting a dataflow
customizes the ultrasound system to work according to the
services associated with the selected dataflow.
5. Button: allows you to assign a pre-configured output
service (or a set of output services) to the Print keys on the
control panel.
6. Removable Media: enables formatting (DICOM, database,
or blank formatting) and DICOM verification of removable
media.
7. Miscellaneous: allows you to set up the patient exam
menu options, print and store options, and the order of the
columns in the examination list on the Patient menu.
Configure these screens from left to right, starting with the
Tcpip tab first.
NOTE: The ultrasound system is pre-configured for many services, with
default settings selected. You can change these services and
settings as needed.
CAUTION You must restart the LOGIQ e after making any changes to
connectivity settings in the Utility menus. This includes any
changes on the TCPIP - Device Properties or dataflow setup
screens.

Accessing Documentation Via a PC

To view user documentation on a PC,
1. Insert the media into the media drive.
2. Open the media 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 Adobe Reader, a free download is
available on the Adobe website at http://www.adobe.com.

Using Online Help Via F1

Online Help is available via the F1 key. After pressing F1, Help
appears. 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), and the
content portion on the right side of the screen where help topics
are displayed.
NOTE: If the cursor is lost while using Online Help, press Alt + F4 to
exit or press F1 to activate the cursor.
Figure 3-8. Opening Help Screen
Exiting Online Help
To exit Online Help, press the ‘X’ in the upper, right-hand corner
of the Online Help window.

Contact Information
Contacting GE Healthcare Ultrasound

For additional information or assistance, please contact your
local distributor or the appropriate support resource listed on the
following pages:
INTERNET http://www.gehealthcare.com
http://www.gehealthcare.com/usen/ultrasound/products/
probe_care.html
USA GE Healthcare TEL: (1) 800-437-1171
Ultrasound Service Engineering FAX: (1) 414-721-3865
9900 Innovation Drive
Wauwatosa, WI 53226
Clinical Questions
For information in the United States, Canada, Mexico and parts
of the Caribbean, call the Customer Answer Center
TEL: (1) 800-682-5327 or (1) 262-524-5698
In other locations, contact your local Applications, Sales or
Service Representative.
Service Questions For service in the United States, call GE CARES
TEL: (1) 800-437-1171
For service for compact products in the United States, call
TEL: (1) 877-800-6776
In other locations, contact your local Service Representative.
Accessories To request the latest GE Accessories catalog or equipment
Catalog Requests brochures in the United States, call the Response Center
TEL: (1) 800-643-6439

Contacting GE Healthcare Ultrasound (continued)

Contact Information
Placing an Order To place an order, order supplies or ask an accessory-related

question in the United States, call the GE Access Center
TEL: (1) 800-472-3666
CANADA
GE Healthcare TEL: (1) 800-668-0732
Ultrasound Service Engineering
Wauwatosa, WI 53226
Customer Answer Center TEL: (1) 262-524-5698
LATIN & SOUTH GE Healthcare TEL: (1) 262-524-5300
AMERICA Ultrasound Service Engineering
Wauwatosa, WI 53226
Customer Answer Center TEL: (1) 262-524-5698
EUROPE GE Ultraschall TEL: 0130 81 6370 toll free
Deutschland GmbH & Co. KG TEL: (33) 130.831.300
Beethovenstrasse 239 FAX: (49) 212.28.02.431
Postfach 11 05 60
D-42655 Solingen
ASIA
GE Ultrasound Asia (Singapore) TEL: 65-291 8528
Service Department - Ultrasound FAX: 65-272-3997
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730
JAPAN GE Healthcare Japan Corporation TEL: (81) 42-648-2910

Customer Service Center FAX: (81) 42-648-2905
ARGENTINA GEME S.A. TEL: (1) 639-1619

Miranda 5237 FAX: (1) 567-2678
Buenos Aires - 1407

AUSTRIA
GE GesmbH Medical Systems Austria TEL: 0660 8459 toll free
Prinz Eugen Strasse 8/8 FAX: +43 1 505 38 74
A-1040 WIEN TLX: 136314
BELGIUM
GE Healthcare BVBA TEL: +32 0 2 719 72 04
Kouterveldstraat 20 FAX: +32 0 2 719 72 05 B-
1831 Diegem
BRAZIL
GE Sistemas Medicos TEL: 0800-122345
Av Nove de Julho 5229 FAX: (011) 3067-8298
01407-907 Sao Paulo SP
CHINA
GE Healthcare - Asia TEL: (8610) 5806 9403
No. 1, Yongchang North Road FAX: (8610) 6787 1162
Beijing Economic & Technology Development Area
Beijing 100176, China
DENMARK
GE Medical Systems TEL: +45 4348 5400
Fabriksparken 20 FAX: +45 4348 5399
DK-2600 GLOSTRUP
FRANCE
GE Medical Systems TEL: 05 49 33 71 toll free
738 rue Yves Carmen FAX: +33 1 46 10 01 20
F-92658 BOULOGNE CEDEX
GERMANY GE Ultraschall TEL: 0130 81 6370 toll free
Deutschland GmbH & Co. KG TEL: (49) 212.28.02.207
Beethovenstrasse 239 FAX: (49) 212.28.02.431
Postfach 11 05 60
D-42655 Solingen
GREECE
GE Medical Systems Hellas TEL: +30 1 93 24 582
41, Nikolaou Plastira Street FAX: +30 1 93 58 414
G-171 21 NEA SMYRNI
ITALY
GE Medical Systems Italia TEL: 1678 744 73 toll free
Via Monte Albenza 9 FAX: +39 39 73 37 86
I-20052 MONZA TLX: 3333 28
LUXEMBOURG TEL: 0800 2603 toll free

Contact Information


MEXICO GE Sistemas Medicos de Mexico S.A. de C.V.
Rio Lerma #302, 1° y 2° Pisos TEL: (5) 228-9600
Colonia Cuauhtemoc FAX: (5) 211-4631 06500-
Mexico, D.F.
NETHERLANDS
GE Medical Systems Nederland B.V. TEL: 06 022 3797 toll free
Atoomweg 512 FAX: +31 304 11702
NL-3542 AB UTRECHT
POLAND
GE Medical Systems Polska TEL: +48 2 625 59 62
Krzywickiego 34 FAX: +48 2 615 59 66
P-02-078 WARSZAWA
PORTUGAL GE Medical Systems Portuguesa S.A.
TEL: 05 05 33 7313 toll free
Rua Sa da Bandeira, 585 FAX: +351 2 2084494
Apartado 4094 TLX: 22804
P-4002 PORTO CODEX
RUSSIA
GE VNIIEM TEL: +7 495 739 6931
18C, Krasnopresnenskaya nab. FAX: +7 495 739 6932
MOSCOW 123317 TLX: 613020 GEMED SU
SPAIN GE Healthcare TEL: +34 (91) 663 25 00
Edificio Gobelas I FAX: +34 (91) 663 25 01
C/ Gobelas 35-37
E- 28023-Madrid
SWEDEN GE Medical Systems TEL: 020 795 433 toll free
PO-BOX 1243 FAX: +46 87 51 30 90
S-16428 KISTA TLX: 12228 CGRSWES
SWITZERLAND
GE Medical Systems (Schweiz) AG TEL: 155 5306 toll free
Sternmattweg 1 FAX: +41 41 421859
CH-6010 KRIENS
TURKEY GE Healthcare Turkiye TEL: +90 212 366 29 00
Sun Plaza FAX: +90 212 366 29 99
Dereboyu Sok. No 24/7
34398 Maslak
ISTANBUL

UNITED KINGDOM GE Medical Systems TEL: 0800 89 7905 toll free
Coolidge House FAX: +44 753 696067
352 Buckingham Avenue
SLOUGH
Berkshire SL1 4ER
OTHER NO TOLL FREE TEL: international code + 33 1 39 20 0007
COUNTRIES
Manufacturer
GE Medical Systems (China) Co., Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688
Factory Sites
GE Medical Systems (China) Co.,
Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development
Zone
Jiangsu, P.R. China
214028
TEL: +86 510 85225888; FAX: +86 510 85226688
GE Medical Systems
Ultrasound & Primary Care
Diagnostics, LLC
Also DBA GE Healthcare
Wauwatosa, WI 53226
U.S.A

Inspecting the System

Examine the following on a monthly basis:
• Connectors on cables for any mechanical defects.
• Entire length of electrical and power cables for cuts or abrasions.
• Equipment for loose or missing hardware.
• Control panel and keyboard for defects.
• Casters for proper locking operation.
CAUTION To avoid electrical shock hazard, do not remove panels or

covers from console. This servicing must be performed by
qualified service personnel. Failure to do so could cause
serious injury.
Biological If any defects are observed or malfunctions occur, do not

Hazard operate the equipment but inform a qualified service person.
Contact a Service Representative for information.

Weekly Maintenance
Failure to perform required maintenance may result in
unnecessary service calls.
Prior to cleaning any part of the system:
1. Turn off the system power. If possible, disconnect the power
cord. See ‘Power Off’ on page 1-19 for more information.
System Cabinet
To clean the system cabinet:

1. Moisten a soft, non-abrasive folded cloth.
2. Wipe down the top, front, back, and both sides of the
system cabinet.
NOTE: Do not spray any liquid directly into the unit.
LCD Monitor
To clean the monitor face:

Use a soft, folded cloth. Gently wipe the monitor face.
Do NOT use a glass cleaner that has a hydrocarbon base (such
as Benzene, Methyl Alcohol or Methyl Ethyl Ketone) on monitors
with the filter (anti-glare shield). Hard rubbing will also damage
the filter.
NOTE: When cleaning the screen, make sure not to scratch the LCD.
Operator Controls
To clean the operator control panel:

1. Moisten a soft, non-abrasive folded cloth with a mild,
general purpose, non-abrasive soap and water solution.
2. Wipe down operator control panel.
3. Use a cotton swab to clean around keys or controls. Use a
toothpick to remove solids from between keys and controls.
NOTE: When cleaning the operator control panel, make sure not to spill
or spray any liquid on the controls, into the system cabinet, or in
the probe connection receptacle.

NOTE: In case of SARS, use bleach, alcohol, or Cidex in a normal
diluted form for cleaning/disinfecting the operator panel.
NOTE: DO NOT use T-spray or Sani Wipes on the control panel.

Touch Screen
To clean the Touch Screen, moisten a soft, non-abrasive folded

cloth with lukewarm water and wipe the external surface. It can
also be wiped by using the Sani-cloth HB.
Replacing illuminated key caps/lamps
Contact a local Service Representative when a key cap or lamp

needs to be replaced.
Other Peripheral Maintenance
Refer to the peripheral manuals for more information.

Other Maintenance
Optimum Ultrasound system performance is your facility’s
responsibility. Ensure that your facility establishes a regular
maintenance program at the appropriate time intervals to
perform the following tasks:
• inspect the system, probes, and peripherals
• clean system parts
• test leakage current
• verify measurement accuracy
• assure probe quality with phantom checks
Your facility’s Biomedical Department may perform this service;
or contact the GE Service Representative to verify/contract for
coverage.
Battery Replacement and Disposition
Battery replacement every three years is recommended.

Contact a local Service Representative for the replacement of
the battery. Used batteries will be discarded appropriately by
NOTE: Disposing of the battery should meet local law and regulatory
requirements.
NOTE: Dispose of the system according to local law and regulatory
requirements.
GE.

Supplies/Accessories
CAUTION DO NOT connect any probes or accessories without approval

by GE.
Not all features or products described in this document may be

available or cleared for sale in all markets.
The following supplies/accessories have been verified to be
compatible with the system:
Peripherals
Table 3-2: Peripherals and Accessories

Accessory Units
Sony B/W Printer Each
Sony Digital Color Printer Each
HP470 Printer Each
HP 8600 PC Printer Each
DVD R/W Each
USB Wireless Card Each
Measure Transfer Kit Each
USB Memory Stick Each
USB Hub Assy Each
ECG-USB Each
USB HDD Each
Docking Cart Each
BarCode Reader Each
Sandisk U3 USB Flash Drive Each

Video Transfer Each
Console
Table 3-3: Console Accessories
Accessory Units
Footswitch model FSU-1000 Each
Footswitch model MKF 2- MED GP26 Each
Battery Pack model Each
Probes
Table 3-4: Probes and Accessories

Accessory Units
4C-RS Each
8C-RS Each
E8C-RS Each
8L-RS Each
9L-RS Each
12L-RS Each
16L-RS Each
i12L-RS Each
3S-RS Each
i739-RS/t739-RS Each
*6Tc-RS Each
*6S-RS Each
NOTE: 16L-RS is not available in China

*NOTE: LOGIQ e R6.x.x only

Gel
Table 3-5: Gel
Accessory Units
Thermasonic Gel Warmer

Holds three plastic bottles
(250ml or 8 oz)
Aquasonic 100 Scan Gel

5 liter jug
250 ml plastic bottles (12/

case)
Scan Ultrasound Gel 8 oz plastic bottles (12/

case)
1 gallon plastic jug
Four 1-gallon plastic jugs
Disinfectant
Table 3-6: Disinfectant
Accessory Units
Cidex Activated Dialdehyde 16/1 quart bottles
4/1 gallon bottles
2/2.5 gallon bottles

Ultrasound Probe and Cord Sheath Sets
Table 3-7: Probe and Cord Sheath Sets
Accessory Units
Sterile Ultrasound Probe Sheath Set 20 Per Set
Sterile Ultrasound Cord Sheath Set 20 Per Set

Sanitary Rectal/Vaginal Probe Cover 20 Per Set
Sterile Combination Probe and Cord Cover Set 12 Per Set
Sterile Ultrasound Probe Sheath Set for Wide (2.5 and 3.5) 20 Per Set
Aperture Sector Probes


Chapter 4
Safety
Describes the safety and regulatory information

pertinent for operating this ultrasound system.

Safety
Safety Precautions
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.
CAUTION Indicates that a potential hazard may exist which through

inappropriate conditions or actions will or can cause:
• 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.

Safety Precautions
Hazard Symbols
Icon Description
Potential hazards are indicated by the following icons:
Table 4-1: Potential Hazards
Icon Potential Hazard Usage Source
• Patient/user infection due to ISO 7000

• Cleaning and care
contaminated equipment. No. 0659
instructions
• Sheath and glove
guidelines
• Electrical micro-shock to patient, e.g., • Probes

ventricular • ECG, if applicable
• Connections to back
panel
• Patient injury or tissue damage from • ALARA, the use of

ultrasound radiation. Power Output following
the ‘as low as
reasonably
achievable’ principle
• Risk of explosion if used in the • Flammable anesthetic

presence of flammable anesthetics.
• Patient/user injury or adverse reaction • Replacing fuses

from fire or smoke. • Outlet guidelines
• Patient/user injury from explosion and
fire.
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.

Safety
CAUTION Improper use can result in serious injury. The user must be
thoroughly familiar with the instructions and potential hazards
involving ultrasound 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.

Safety Precautions
Patient Safety
Related Hazards
WARNING The concerns listed can seriously affect the safety of patients
undergoing a diagnostic ultrasound examination.
Patient Always include proper identification with all patient data and
identification verify the accuracy of the patient's name and 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.
If the LOGIQ e needs to be sent for repair, ensure that any
patient information is backup and erased from the system
before shipping. In case that any patient information is still
residing on the LOGIQ e, GE will contact the customer and
request for urgent collection of that patient information. GE will
keep this patient information in a secure environment for a
maximum period of 1 month. All patient information will be
permanently deleted at that point.
Diagnostic Equipment malfunction or incorrect settings can result in
information 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.
Related Hazards (continued)
Mechanical The use of damaged probes can result in injury or increased risk
hazards 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.

Safety
Electrical
Hazard A damaged probe can also increase the risk of electric shock if
conductive solutions come in contact with internal live parts.
Inspect probes 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.
CAUTION Ultrasound transducers are sensitive instruments which can
easily be damaged by rough handling. Take extra care not to
drop 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.
CAUTION Ultrasound can produce harmful effects in tissue and potentially

result in patient injury. Always minimize exposure time and
keep 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.
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 Precautions
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 e.
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

Hazard anesthetics.
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 (having

Safety
equalization conductor ).
Never use any adaptor or converter of a three-prong-
•totwo-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.
CAUTION Do not use this equipment if a safety problem is known to exist.
Have the unit repaired and performance verified by qualified
service personnel before returning to use.
Smoke & The system must be supplied from an adequately rated

Fire Hazard electrical circuit. The capacity of the supply circuit must be as
specified.
Biological For patient and personnel safety, be aware of biological

Hazard hazards while performing invasive procedures. To avoid the
risk of disease 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 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.
CAUTION Contact with natural rubber latex may cause a severe

anaphylactic reaction in persons sensitive to the natural latex
protein. Sensitive 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.

Safety Precautions
CAUTION Archived data is managed at the individual sites. Performing
data backup (to any device) is recommended.
CAUTION DO NOT use high-frequency surgical equipment with the

LOGIQ e.

Safety
General Caution
CAUTION Standard maintenance must be performed by authorized

service personnel for the lifetime of the product (7 years).
CAUTION Proceed cautiously when crossing door or elevator thresholds

with the Docking Cart or Isolation Cart. Use the handle to push/
pull the system, e.g., do not use the Docking Cart external LCD.
Failure to do so may cause serious injury or system damage.
CAUTION Capacity load of the Docking Cart: The maximum capacity load
of the Storage rack (1) is 2kg, DVD-RW Shelf (2) is 2kg, B/W
Printer Shelf (3) is 4kg, Color Printer Shelf (4) is 7kg, and UPS
Shelf (5) is 9kg, refer to the following figure.
Figure 4-1. Capacity load of the Docking Cart

Safety Precautions
General Caution (continued)
CAUTION Capacity load of the Isolation Cart: The maximum capacity load
of B/W Printer (1) is 4kg, Color Printer Shelf (2) is 7kg, DVDRW
Shelf (3) is 2kg and Bottom Shelf (4) is 6kg, refer to the
following figure.
Figure 4-2. Capacity load of the Isolation Cart

Safety
General Caution (continued)
CAUTION Capacity load of the Isolation Cart Enhanced Version: The

maximum capacity load of Basket (1) and Drawer (5) is 3kg,
ACDC Shelf (2) is 1.5kg, DVD-RW Shelf (3) is 1.5kg and B/W
Printer Shelf (4) is 3kg, refer to the following figure.
Figure 4-3. Capacity load of the Isolation Cart Enhanced

Version
Device Labels
Label Icon Description
The following table describes the purpose and location of safety

labels and other important information provided on the
equipment.

Safety Precautions
Table 4-2: Label Icons
Label/Icon Purpose/Meaning Location
Identification and Rating Plate • Manufacture’s name and AC Adapter Label.

address
• Date of manufacture
• 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 Bottom of Footswitch

IPX8: MKF 2-MED GP26, provided by the enclosure per
FSU1000 IEC60 529.
IPX8 can be used in an operating
room environment.
Authorized European
Representative address.
United States only

Prescription Requirement label.
Type BF Applied Part (man in the Beside the probe connector

box) symbol is in accordance
with IEC 878-02-03.
General Warning. Various
Various
“CAUTION” - Dangerous voltage”
(the lightning flash with
arrowhead) is used to indicate
electric shock hazards.

Safety
Table 4-2: Label Icons (Continued)
“ON” indicates the power on See the Console Overview

position of the power switch. section for location information.
CAUTION: This Power Switch
DOES NOT ISOLATE Mains
Supply.
“Protective Earth” indicates the Inside of AC adapter

protective earth (grounding)
terminal.
NRTL Listing and Certification Bottom

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.
ECG Module
Type CF Defib-Proof Applied
Part (heart in the box with paddle)
symbol is in accordance with IEC
60878-02-06.
“Consult accompanying Various

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.
Do not push the system. Rear of Docking Cart/Isolation

Cart

Safety Precautions

This symbol indicates that waste Bottom
electrical and electronic
equipment must not be disposed
of as unsorted municipal waste
and must be collected
separately. Please contact an
authorized
representative of the
manufacturer for information
concerning the decommissioning
of your equipment.
The separate collection symbol is Battery Pack if contains Pb/Cd/

affixed to a battery, or its Hg
packaging, to advise you that the
battery must be recycled or
disposed of in accordance with
local or country laws. The letters
below the separate collection
symbol indicate whether certain
elements
(Pb=Lead,Cd=Cadmium,
Hg=Mercury) are contained in the
battery. To minimize potential
effects on the environment and
human health, it is important that
all marked batteries that you
remove from the product are
properly recycled or disposed.
For information on how the
battery may be safely removed
from the device, please consult
the service manual or equipment
instructions.Information on the
potential effects on the
environment and human health
of the substances used in
batteries is available at this url:
http://
www.gehealthcare.com/euen/
weee-recycling/index.html

Safety

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 Probe and Rear Panel, China

hazardous substance(s) above Rating Plate
the maximum concentration
value. Maximum concentration
values for electronic information
products, as set by the People’s
Republic of China Electronic
Industry Standard
SJ/T113642006, 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.
When closing the LCD cover, use Bottom
caution to avoid injuring hands or
fingers as there is a closing
mechanism which allows the
LCD cover to automatically close.

Safety Precautions

Do not connect the DVD-RW to DVD-RW
the system while scanning.
The DVD-RW can be used when
connecting to the Docking Cart.
GOST symbol: Russia Bottom

Regulatory Country Clearance.
This product consists of devices Bottom

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

Safety
Label Icon Description (continued)
Classifications Type of protection against electric shock

• Class I Equipment
• LOGIQ e Console with AC Adapter (*1)
• Docking Cart Console
Degree of protection against electric shock
Type BF Applied part (*2)

• (for Probes marked with BF symbol)
• Type CF Applied part (*3) (for ECG marked with CF symbol)
Continuous Operation
System is Ordinary Equipment (IPX0)
Footswitch is IPX8 (FSU-1000, MKF 2-MED GP26)
*1. Class I Equipment
EQUIPMENT in which protection against electric shock does not
rely on BASIC INSULATION only, but includes a protective 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 4-3: 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 4-4: Type CF Equipment
Normal Mode Single fault condition

Safety Precautions
Patient leakage current Less than 10 microA Less than 50 microA
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 Medical Devices Directive as
stated in EN 60601-1-2. 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
EMC Performance for a Class A FCC Device, 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 FCC
regulations.
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.

Safety
EMC Performance (continued)
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.
CAUTION Do not use devices which intentionally transmit RF signals

(cellular phones, transceivers, or radio controlled products),
other than those supplied by GE (wireless microphone,
broadband over power lines, 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.
EMC Performance (continued)
Portable and mobile radio communications equipment (e.g.

twoway radio, cellular/cordless telephones and similar
equipment) should be used no closer to any part of this system,
including cables, than determined according to the following
method:

Safety Precautions
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 (e.g. three-
prong-to-twoprong 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 (e.g. 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 in Chapter 18 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

Safety
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)

Safety Precautions
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 e to image recording and other devices or
communication networks.
Peripheral used in The LOGIQ e has been verified for overall safety, compatibility
the patient and compliance with the following on-board image recording
environment devices:
• Sony UP-D897 B/W Printer
• Sony UP-D25MD Color Printer
The LOGIQ e 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.
CAUTION The connection of equipment or transmission networks other
than as specified in the user instructions can result in an
electric shock 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.
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. There must be adequate mechanical mounting of the
device and stability of the combination.
3. Risk and leakage current of the combination must comply
with IEC/EN 60601-1-1.
4. Electromagnetic emissions and immunity of the
combination must conform to IEC/EN 60601-1-2.
Peripheral Update for EC countries (continued)
Peripheral used in The LOGIQ e has also been verified for compatibility, and
the non-patient compliance for connection to a local area network (LAN) via a
environment wireless LAN, provided the LAN components are IEC/EN 60950
compliant.
The LOGIQ e has also been verified for compatibility, and
compliance for connection to a DVD-RW via the system USB
port, provided the DVD-RW is IEC/EN 60950 compliant.

Safety
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.

Safety Precautions
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 4-5: Declaration of Emissions

Guidance and manufacturer’s declaration - electromagnetic emissions
The system is intended for use in the electrmagnetic 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.
CISPR 11 Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF Emissions Class A
CISPR 11
This system is suitable for use in all establishments, other than
domestic establishments and those directly connected to the
public low-voltage power supply network that supplies buildings
Harmonic Class A used for domestic purposes, provided the following warning is
Emissions heeded:
IEC 61000-3-2 WARNING: This system is intended for use by healthcare
Voltage Complies professionals only. This system may cause radio interference or
Fluctuations/Flicker may disrupt the operation of nearby equipment. It may be
Emissions necessary to take mitigation measures, such as re-orienting or
IEC 61000-3-3 relocating the system or shielding the location.
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 4-6: Declaration of Immunity

Immunity Equipment Regulatory EMC Environment and
Type Capability Acceptable Level Guidance
IEC 61000-4-2 ± 6 kV contact ± 6 kV contact
Static discharge
(ESD) ± 8 kV air ± 8 kV air Floors should be wood, concrete, or
ceramic tile. If floors are covered with
synthetic material, the relative
humidity should be at least 30%.
IEC 61000-4-4 ± 2 kV for mains ± 2 kV for mains Mains power quality should be that of
Electrical fast a typical commercial and/or hospital
transient/burst ± 1 kV for SIP/ ± 1 kV for SIP/SOP environment. If the user requires
SOP continued operation during power

Safety
IEC 61000-4-5 ± 1 kV differential ± 1 kV differential mains interruptions, it is
Surge Immunity recommended that the system be
± 2 kV common ± 2 kV common powered from a UPS or a battery.
NOTE: UT is the a.c. mains voltage
IEC 61000-4-11 < 50T (> 95% dip) < 50T (> 95% dip) for prior to application of the test level.
Voltage dips, for 0.5 cycle; 400T 0.5 cycle; Power frequency magnetic fields
short (60 0ip) for 5 400T (60 0ip) for 5 should be at levels characteristic of a
interruptions typical location in a typical commercial
cycles; cycles;
and voltage and/or hospital environment.
variations on 700T (30 0ip) for 700T (30 0ip) for 25 Separation distance to radio
mains supply 25 cycles; cycles; communication equipment must be
< 50T (>95% dip) < 50T (>95% dip) for 5 maintained according to the method
for 5 sec sec below. Interference may occur in the
IEC 61000-4-8 3 A/m 3 A/m vicinity of equipment marked with the
Power symbol:
frequency (50/
60 Hz) magnetic
field
Image degradation or interference
may occur due to conducted RF noise
V V
IEC 61000-4-6 3 RMS 3 RMS on the equipment mains power supply
Conducted RF 150 kHz - 80 MHz 150 kHz - 80 MHz or other signal cable. Such
interference is easily recognized and
IEC 61000-4-3 3 V/m 3 V/m
distinguishable from patient anatomy
Radiated RF 80 MHz - 2.5 GHz 80 MHz - 2.5 GHz
and physiological waveforms.
Interference of this type may delay the
examination without affecting
diagnostic accuracy. Additional mains/
signal RF isolation or filtering may be
needed if this type interference occurs
frequently.
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.

Safety Precautions
Patient Environmental Devices
Figure 4-4. Patient Environmental Devices
1. Left side:
• 2 USB Ports—Peripheral devices, Printers (Color and
USB), Memory Stick, Footswitch, Wireless LAN
Adapter, USB Hub, ECG, USB HDD
• 1 Earphone Port
2. Bottom side: Lithium-ion battery port
3. Right side: Probe port, Security lock
4. Rear panel:
• 1 VGA Port.
• 1 Network Port
• 1 Docking Port
Acceptable Devices
The Patient Environmental devices shown on the previous page

are specified to be suitable for use within the PATIENT
ENVIRONMENT.

Safety
CAUTION DO NOT connect any probes or accessories without approval
by GE within the PATIENT ENVIRONMENT.
See ‘Peripheral Update for EC countries’ on page 4-24 for more
information.
Unapproved Devices
CAUTION DO NOT use unapproved devices.

If devices are connected without the approval of GE, the
warranty will be INVALID.
Any device connected to the LOGIQ e 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
CAUTION Unsafe operation or malfunction may result. Use only the

accessories, options and supplies approved or recommended
in these instructions for use.
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.

Safety Precautions
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.
Acoustic Output Display Specifications (continued)
Mechanical Index MI 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.
Changing the You can select the displayed TI type on Utility -> Imaging ->
Thermal Index BMode. This preset is application dependent so each
Type application could specify a different TI type.
Display precision is ±0.1 and accuracy is ±50%. Accuracy of the
power output displayed value on the Top/Sub Menu is ±2% in B-
and M-Modes and ±10% in all other modes.
Controls Affecting Acoustic Output
The potential for producing mechanical bioeffects (MI) or

thermal bioeffects (TI) can be influenced by certain controls.
Direct. The Acoustic Output control has the most significant
effect on Acoustic Output.
Indirect. Indirect effects may occur when adjusting controls.
Controls that can influence MI and TI are detailed under the
Bioeffects portion of each control in the Optimizing the Image
chapter.
Always observe the Acoustic Output display for possible
effects.

Safety
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 sections in 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
Output diagnostic image or measurement during an examination.
Hazard Begin the exam with the probe that provides an optimum focal
depth and penetration.
Acoustic Output Default Levels
In order to assure that an exam does not start at a high output

level, the LOGIQ e initiates 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.
To modify acoustic output, adjust the Power Output level on the
Top/Sub Menu.
Warning Label Locations
LOGIQ e warning labels are provided in English.

Safety Precautions
Figure 4-5. Label location

1. “Consult accompanying document“ is intended the published specifications. Keep power to
to alert the user to refer to the operator manual these devices turned off when near this
or other instructions when complete equipment.
information cannot be provided on the label. 4. Be careful of static
2. Possible shock hazard. Do not remove covers 5. Prescription Device (For U.S.A. Only)
or panels. No user serviceable parts are 6. WEEE Label
inside. Refer servicing to qualified service 7. The CE Mark of Conformity indicates this
personnel. equipment conforms with the Council Directive
3. Do not use the following devices near this 93/42/EEC.
equipment: cellular phone, radio receiver, 8. CISPR CAUTION: The LOGIQ e conforms to
mobile radio transmitter, radio controlled toy, the CISPR11, Group 1, Class A of the
etc. Use of these devices near this equipment international standard for Electromagnetic
could cause this equipment to perform outside disturbance characteristics.

Safety
Warning Label Locations (continued)
Figure 4-6. Docking Cart Rating Plate

Safety Precautions
Figure 4-7. LOGIQ e R5.2.x TUV and

Identification/Rating Plate Label Location
Table 4-7: Rating Plate Explanations

Date of manufacture: The date could
be a year, year and month, or year,
month and day, as appropriate. See ISO
8601 for date formats.
Catalog or model number
REF
Serial number
SN

Safety
Direct Current: For products to be
powered from a DC supply
Input
Table 4-7: Rating Plate Explanations

For use with adapter model TWADP100
Description

Safety Precautions
Figure 4-8. LOGIQ e R5.2.x Rating Plate (China only)
Figure 4-9. LOGIQ e R6.x.x TUV and Identification/Rating

Plate Label Location

Safety
Figure 4-10. LOGIQ e R6.x.x Rating Plate (China only)
Figure 4-11. LOGIQ e Rating Plate (CKD version)

Safety Precautions
Figure 4-12. AC Adapter Label

Safety
Figure 4-13. Battery Label
1. Do not put the battery in fire.

2. Do not disassemble or mistreat the battery.
CAUTION Do not disassemble or mistreat the battery. Do not put the

battery in fire. Replace the battery with the same battery type
only. Failure to follow these instructions many present risk of
explosion fire or high temperature. See the battery user
manual for additional safety instructions.

Chapter 5
Emergency Department (ED)
Describes the LOGIQ e system for use in the

Emergency Department.

Beginning an Exam
Introduction
You optimize the image on the LOGIQ e Emergency Department
system by adjusting the Depth (with Auto Focus Zone and
Frequency) control. Further optimization should not be required
though manual adjustment is allowed.
‘ED’ appears on the lower right and corner of the display screen.

Beginning an Exam
Starting a New Patient

Press Patient.
Figure 5-1. ED Patient Screen
Refer to Beginning an Exam in Chapter 2.

B-Mode
Intended Uses
B-Mode is intended to provide two-dimensional images and

measurement capabilities concerning the anatomical structure
of soft tissue.
Figure 5-2. B-Mode Display

B-Mode Top/Sub Menu
Adjust the image by using the Depth control. If additional

functionality is needed, the following Top/Sub Menu controls are
available.
See Chapter 2 for more details on these controls.
Figure 5-3. B-Mode Top/Sub Menu

M-Mode
Intended Use
M-Mode is intended to provide a display format and

measurement capability that represents tissue displacement
(motion) occurring over time along a single vector.
Figure 5-4. M-Mode Top/Sub Menu
M-Mode Top/Sub Menu
The following Top/Sub Menu controls are available for

functionality adjustment and image optimization.
Figure 5-5. M-Mode Top/Sub Menu

Color Flow (CF) Mode
Intended Use
Color Flow Mode is a Doppler Mode intended to add

colorcoded qualitative information concerning the relative
velocity and direction of fluid motion within the B-Mode image.
Figure 5-6. Color Flow Mode Display


CF-Mode Top/Sub Menu
Figure 5-7. CF-Mode Top/Sub Menu

Power Doppler Imaging (PDI) Mode
Intended Uses
Power Doppler Imaging (PDI) 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. Using this technique, the ultrasound system plots color
flow based on the number of reflectors that are moving,
regardless of their velocity. PDI does not map velocity,
therefore it is not subject to aliasing.


Figure 5-8. Power Doppler Imaging Display
PDI Top/Sub Menu
Figure 5-9. PDI Top/Sub Menu

M Color Flow Mode
Intended Uses
M Color Flow is used for fetal cardiac applications. Color Flow

overlays color on the M-Mode image using velocity and variance
color maps. The Color Flow wedge overlays the B-Mode image
and M-Mode timeline.
Figure 5-10. M Color Flow Display


M Color Flow Top/Sub Menu
Figure 5-11. M Color Flow Top/Sub Menu

Pulsed Wave (PW) Doppler Mode
Intended Use
Doppler is intended to provide measurement data concerning

the velocity of moving tissues and fluids. PW Doppler lets you
examine blood flow data selectively from a small region called
the sample volume.
Figure 5-12. Doppler Mode Display


PW Doppler Mode Top/Sub Menu
Figure 5-13. PW Doppler Mode Top/Sub Menu

Chapter 6
Nerve Block
Describes the LOGIQ e system for use in regional

anesthesia guidance.

Nerve Block
Beginning an Exam
Introduction
You optimize the image on the LOGIQ e Nerve Block system,
adjust the image by adjusting the Depth (with Auto Focus Zone
and Frequency) control. Further optimization should not be
required though manual adjustment is allowed.
‘NERVE’ appears on the lower right and corner of the display
screen.

Beginning an Exam

Press Patient.
Figure 6-1. Nerve Block Patient Screen

Nerve Block
Refer to Beginning an Exam in Chapter 2.
Selecting an Application Preset and a Probe
Figure 6-2. Nerve Application Preset

B-Mode
Intended Uses

Nerve Block
B-Mode Top/Sub Menu
Adjust the image by using the Depth control. If additional

functionality is needed, the following Top/Sub Menu controls are
available.
Figure 6-4. B-Mode Top/Sub Menu

Intended Uses
Color Flow Mode is a Doppler Mode intended to add colorcoded

qualitative information concerning the relative velocity and
direction of fluid motion within the B-Mode image.

Nerve Block

CF-Mode Top/Sub Menu
Figure 6-6. CF-Mode Top/Sub Menu

Intended Uses
Power Doppler Imaging (PDI) 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. Using this technique, the ultrasound system plots color
flow based on the number of reflectors that are moving,
regardless of their velocity. PDI does not map velocity,
therefore it is not subject to aliasing.

Nerve Block

PDI Top/Sub Menu
Figure 6-8. PDI Top/Sub Menu

Intended Use

the sample volume.
Figure 6-9. Doppler Mode Display

Nerve Block

PW Doppler Mode Top/Sub Menu
Figure 6-10. PW Doppler Mode Top/Sub Menu

Chapter 7
Using Touch
Screen
Describes the use of the Touch Screen with the LOGIQ

e system.

Using Touch Screen
Beginning an Exam
Introduction
Activate/Deactivate Touch Screen mode by pressing F12.
NOTE: All the function keys except F12, Cursor, Set/B Pause, Power
Key and keyboard of LOGIQ e will be disabled if Touch Screen
mode is activated.
NOTE: Pressing the Power key automatically deactivates the Touch
Screen Mode.
NOTE: Always use fingers or gloved fingers to operate on the Touch
Screen, improper use may cause damage to the monitor.
NOTE: It is recommended to close the LOGIQ e LCD after activating the
Touch Screen mode to avoid keyboard contamination of blood,
chemicals, etc.

Beginning an Exam

Using Touch Screen
Touch Screen Display

Figure 7-1. Touch Screen Display Tour
1. Patient, click to register patient 10. Freeze
2. Preset, click to go into Preset Screen 11. P1, P3, click to store images
3. Comment, click to add comments 12. Power Output
4. Measure, click to start 2D measurement 13. Focus Position Control
5. End Exam, click to end current exam and 14. Depth Control
system will auto store images permanently. 15. Frequency Control
6. B Pause, click to toggle between real time 16. Gain Control, click fast forward to increase or
BMode with Doppler Mode (with audio) fast backward to decrease gain by larger
7. Clear All, click to clear all the annotations an steps
measurements. 17. Scroll Button, click to go to previous/next
8. Mode Panel Bar, click to select mode. clipboard gallery
9. Top Menu
Press the Patient Touch Screen key, a patient ID will be auto
generated, and begins a new exam.
Selecting an Application Preset and a Probe

Press the Preset Touch Screen key to display the Preset
Screen on the monitor. Select the probe or application by
pressing it.

Using Touch Screen
Figure 7-2. Application Preset

B-Mode
Intended Uses
B-Mode is intended to provide two-dimensional images and

measurement capabilities concerning the anatomical structure
of soft tissue.

B-Mode Top Menu
Adjust the image by using the controls on the right. If additional

functionality is needed, the following Top Menu controls are
available.

Using Touch Screen
Figure 7-4. B-Mode Top Menu

M-Mode
Intended Uses
M-Mode is intended to provide a display format and

measurement capability that represents tissue displacement
(motion) occurring over time along a single vector.
Figure 7-5. M-Mode Display
M-Mode Top Menu
The following Top Menu controls are available for functionality

adjustment and image optimization.
Figure 7-6. M-Mode Top Menu

Using Touch Screen
Intended Uses
Color Flow Mode is a Doppler Mode intended to add colorcoded

qualitative information concerning the relative velocity and
direction of fluid motion within the B-Mode image.
CF-Mode Top Menu

Figure 7-8. CF-Mode Top Menu

Intended Uses
Power Doppler Imaging (PDI) 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. Using this
technique, the ultrasound system plots color flow based on the
number of reflectors that are moving, regardless of their
velocity. PDI does not map velocity, therefore it is not subject to
aliasing.
PDI Top Menu


Using Touch Screen
Figure 7-10. PDI Top Menu
Intended Uses

the sample volume.
Figure 7-11. PW Doppler Mode Display
PW Doppler Mode Top Menu

Figure 7-12. PW Doppler Mode Top Menu

Measurement
Measurement
Introduction
Measurement supports 2D caliper only when operating in
Touch Screen mode.
List of General Measurements

The following table shows the types of general measurements
available when you select Measure.
Table 7-1: General Measurements by Mode
If you press Mode

Measure
(while frozen) B and CF Doppler M
Once Distance Velocity Tissue Depth
Twice Time interval
Three Times Time and velocity
General Instructions
The general steps for perform a measurement is as follows:
1. Select the Measure Touch Screen key.
2. Click to place the first caliper .
3. Click to place the second caliper. The result displays in the Results
Window.

Using Touch Screen
Figure 7-13. Measurement example
Figure 7-14. Measurement screen Top Menu
See Chapter 7 for more details of the Top Menu.

Comment

Comment
General Instructions
Clicking Comment initiates the comment mode. Select the
comment in the list, place it by clicking the target position on
the Touch Screen. Click More to select in other applications.
Click Edit to reset cursor position.
Figure 7-15. Comment Screen
Figure 7-16. Comment screen Top Menu

Using Touch Screen
General Instructions (continued)
To reposition a comment,
1. Select Grab Word to select the comment
2. Select the target position on the Touch Screen to reposition.
See Chapter 6 for more details of the Top Menu

Using CINE
Using CINE
Introduction
CINE images are constantly being stored by the system and are
available for playback or manual review via CINE.
Activate CINE
Select Freeze to freeze the image.

Using Touch Screen
CINE mode monitor display
Figure 7-17. CINE mode monitor display
Select Run to go through the image loop. Select Reverse Loop

to go backward frame by frame. Select Forward Loop to go
forward frame by frame.

A contacts clinical questions ,
3-24 Internet , 3-24
accessories ordering , 3-24 service questions , 3-24
requesting a catalog , 3-24 contraindications , 1-3
acoustic output default Control Panel
levels , 4-32 description , 1-13
ALARA (as low as reasonably achievable), Control panel replacing key
bioeffects caps , 3-32 replacing key
, 4-3 lamps , 3-32
area measurements controls keyboard ,
ellipse , 2-14 1-14 operator ,
spline , 2-16 trace 1-13
, 2-15, , 2-16 Touch Panel , 1-14
B D
biological hazards , 4-9 Danger icon, defined , 4-2
B-Mode imaging device labels , 4-14
intended uses , 5-9, , 6-5 devices acceptable , 4-29
B-Mode measurements, general , 2-12 unapproved , 4-29
B-Mode measurements, mode disinfecting probes , 3-6
circumference and area (ellipse) , 2-14 disinfecting solutions, probes , 3-6
circumference and area (spline trace) , 2-16 distance measurement general ,
circumference and area (trace) , 2-15 2-13
distance , 2-13 Doppler measurements, mode
Body Patterns , 2-10 TAMAX and TAMEAN , 2-19
brightness, video , 1-16 time interval , 2-21
velocity , 2-18
C Doppler Mode, general measurements , 2-18
Doppler Mode, PW
Care and maintenance cleaning
intended uses , 5-13, , 6-11
the system monitor , 3-30
operator controls , 3-31
system cabinet , 3-30 E
inspecting the system , 3-29 electrical configurations
maintenance schedule , 3-30 , 1-4
Caution icon, defined , 4-2 electrical hazard , 4-9 electromagnetic
CINE gauge, display location , 1-15 compatiblity (EMC) , 4-19 ellipse
CINE mode measurement, general , 2-14 EMC
activating , 2-9 (electromagnetic compatiblity) , 4-19
circumference measurements equipment safety , 4-8 exam study,
ellipse , 2-14 spline , 2- display location , 1-15
16 trace , 2-15, , 2-16
cleaning probes , 3-4
Color Flow imaging
intended uses , 5-7
Index-1
Index explosion hazard , 4-8
F
Federal law (USA), requirements , 1-3
focal zone, display location , 1-15
freezing an image , 2-9
Connectivity configuring , 3-20 G

overview of screens , 3-20 Gels, coupling , 3-10
presets , 3-20
H
LOGIQ e User Guide
hazards, safety symbols , 4-3 Cord , 1-17 On/Off
hazards, types biological , 4- Standby , 1-18
9 electrical , 4-6, , 4-9 switch, location , 1-18
explosion , 4-8 mechanical , power shut down , 1-19
4-6 I prescription device, caution , 1-3
presets, changing
imaging parameters, display location , 1-15 Connectivity , 3-20 Probe handling
Indications for Use , 1-3 information, and infection control , 3-2 probe
requesting , 3-24 identifier, locating , 1-15 probes cable
handling , 1-22 cleaning , 3-4 connecting
K , 1-20 coupling gels coupling gels,
probes , 3-10
keyboard special keys ,
disconnecting , 1-22
1-14
disinfecting , 3-6
prudent use , 4-2
L
LOGIQ system R
contraindications , 1-3
Results window display location ,
Indications for Use , 1-3
1-15 moving to new location ,
1-15
M
Measurement Summary window, display location , S
1-
safety electromagnetic compatiblity (EMC) , 4-
15
19 equipment , 4-8 hazards , 4-3, , 4-8, ,
measurements, general , 7-11
4-9, , 4-32 smoke and fire , 4-9
M-Mode imaging
labels , 4-14 patient , 4-5 acoustic
intended uses , 5-6
output hazard hazard, types
M-Mode measurements, mode time
acoustic output , 4-6
interval , 2-23 time interval and
electrical hazards , 4-6
velocity , 2-23 tissue depth , 2-
mechanical hazards , 4-6
22
patient identification , 4-5
M-Mode, general measurements , 2-22
patient training, ALARA , 4-7
Monitor , 3-30 moving the system , 1-
personnel , 4-8 precaution
17
icons, defined , 4-2 precaution
levels, defined , 4-2 probes
O handling precautions , 3-2
Operator controls , 3-31 service, requesting , 3-24
system
electrical configurations , 1-4
P power down , 1-19 System
patient safety , 4-5 cabinet , 3-30
T
Index-2 TAMAX and TAMEAN, Doppler mode measurement
auto trace , 2-19 manual trace , 2-19
Power
Time interval
Doppler mode measurement , 2-21
M-Mode measurement , 2-23 time interval and
velocity, M-Mode measurements , 223
Tissue depth, M-Mode measurement , 2-22
Trace measurement, general , 2-15, , 2-16
Trackball functionality status, display location , 1-15
U
LOGIQ e User Guide
3
Utility screens
connectivity , 3-20
V
Velocity, Doppler measurement , 2-18
W
Warning icon, defined , 4-2
Worksheet changing data
, 2-26 viewing , 2-24
Index-3
Index-4
LOGIQ e User Guide


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GE

LOGIQ e User Guide

LOGIQ e complies with regulatory requirements of the following European

GE Healthcare: Telex 3797371

GE Ultraschall: TEL: 49 212.28.02.208

Rev. 1 2008/09/17 Initial release

Rev. 2 2010/04/08 Update for software update and adding probes

List of Effected Pages

Title Page Rev. 3 Chapter 3 Rev. 3

Revision History Rev. 3 Chapter 4 Rev. 3

Regulatory Requirements Rev. 3 Chapter 5 Rev. 3

Table of Contents Rev. 3 Chapter 6 Rev. 3

Chapter 1 Rev. 3 Chapter 7 Rev. 3

Chapter 2 Rev. 3 Index Rev. 3

LOGIQ e User Guide i-1

i-2 LOGIQ e User Guide

LOGIQ e User Guide i-3

Conformance Standards - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2

i-4 LOGIQ e User Guide

LOGIQ e User Guide i-5

i-6 LOGIQ e User Guide

LOGIQ e User Guide i-7

Console Overview, Moving the System, System

LOGIQ e User Guide 1-1

Application Specific Systems

1-2 LOGIQ e User Guide

CAUTION This machine should be used in compliance with law. Some

LOGIQ e User Guide 1-3

1-4 LOGIQ e User Guide

Table 1-1: Example Plug and Outlet Configurations

AC DC Type Specification AC DC Type Specification

220-240 VAC, 2.5A 220-240 VAC, 2.5A

220-240 VAC, 2.5A 220-240 VAC, 2.5A

220-240 VAC, 2.5A 100-120 VAC, 2.5A

220-240 VAC, 2.5A 220-240 VAC, 2.5A

LOGIQ e User Guide 1-5

Figure 1-1. LOGIQ e System (opened view)

1-6 LOGIQ e User Guide

Figure 1-2. LOGIQ e System (side views)

CAUTION For compatibility reasons, use only GE approved probes,

The lithium ion battery provides power when an AC power

LOGIQ e User Guide 1-7

WARNING • The battery has a safety device. Do not disassemble or

1-8 LOGIQ e User Guide

LOGIQ e User Guide 1-9

Figure 1-3. Battery icon

When you select this icon, the following appears:

1-10 LOGIQ e User Guide

Figure 1-4. Battery Status Message

Current power source–displays the current power source, AC

Figure 1-5. Low battery power warning

LOGIQ e User Guide 1-11

1-12 LOGIQ e User Guide

Figure 1-6. Control Panel

LOGIQ e User Guide 1-13

The Top/Sub Menu contains exam function and mode/function

Figure 1-7. Top/Sub Menu Controls

The Top/Sub Menu contains adjustable knobs associated with

The standard alpha-numeric keyboard has some special