GE Logiq 9 User Manual

GE Healthcare
Technical  Publications
Direction 5180302-100
Rev. 1
LOGIQ E9 User Guide
R1.x.x
Operating Documentation
Copyright 2008 By General Electric Co.
0459 

GE Healthcare
Regulatory Requirement
This product complies with regulatory requirements of the following European  
Directive 93/42/EEC concerning medical devices. 
This manual is a reference for the LOGIQ E9. It applies to all versions of the R1.x.x 
software for the LOGIQ E9 ultrasound system. 
0459
GE Medical Systems: 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...

LOGIQ E9 User Guide i-1
Direction 5180302-100 Rev. 1
Revision History
Reason for Change
List of Effective Pages
Please verify that you are using the latest revision of this document. Information 
pertaining to this document is maintained on ePDM (GE Medical Systems 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....

i-2 LOGIQ E9 User Guide
Direction 5180302-100 Rev. 1 This page intentionally left blank. 

LOGIQ E9 User Guide i-3
Direction 5180302-100 Rev. 1
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, with BF 
or CF Applied Parts.
•  According to CISPR 11, LOGIQ E9 system is Group 1, 
Class A (commercial use only).
•  According to IEC 60529, the footswitch rate IPx8 is suitable 
for use...

i-4 LOGIQ E9 User Guide
Direction 5180302-100 Rev. 1
Conformance Standards (continued)
• International Electrotechnical Commission (IEC).
•  IEC/EN 60601-1 Medical Electrical Eqiupment, Part 1 
General Requirements for Safety.
• 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 61157 Declaration of acoustic output parameters.
•  International...

LOGIQ E9 User Guide i-5
Direction 5180302-100 Rev. 1
Country Specific Approval
• JAPAN
MHLW Approved Number: 220ABBZX00177000 

i-6 LOGIQ E9 User Guide
Direction 5180302-100 Rev. 1 

LOGIQ E9 User Guide i-7
Direction 5180302-100 Rev. 1
Table of Contents
Conformance Standards  - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-3
Certifications  - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-4
Original Documentation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-4
Software License Acknowledgements - - - - - - - - - - - - - - - - - - - - - - - - - - i-4
Country Specific Approval - - - - - - - - - -...

i-8 LOGIQ E9 User Guide
Direction 5180302-100 Rev. 1
Measurement and Analysis
B-Mode Measurements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -   2-13
Doppler Mode Measurements  - - - - - - - - - - - - - - - - - - - - - - - - - - - - -  2-25
M-Mode Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -  2-28
Viewing and Editing Worksheets  - - - - - - - - - - - - - - - - - - - - - - - - - - -  2-30
Chapter 3 — After the Exam is Over
Probe Overview
Probe...