GE LOGIQ V2 User Manual page 3

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Revision History
REV
Rev. 1
Rev. 2
Rev. 3
Rev. 4
Rev. 5
Rev. 6
Rev. 7
Rev. 8
Rev. 9
CHAPTER NUMBER
Title Page
Revision History
Regulatory Requirements
Chapter 1
Chapter 2
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop/ePDM (GE 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 V2/LOGIQ V1
Direction 5610736-100 Rev. 9
Reason for Change
DATE
(YYYY/MM/DD)
2015/07/14
2015/10/14
2015/11/23
2015/12/14
2016/02/25
2016/06/14
2016/08/29
2016/12/08
2017/04/25
List of Effective Pages
REVISION
NUMBER
Rev. 9
Rev. 9
Rev. 9
Rev. 9
Rev. 9
User Guide
REASON FOR CHANGE
Initial release
Add onboard help
Remove secure wipe information
Update rating plate
Add intended use
Update rating plate
Add probe UDI label
Update software features
Update onboard help
CHAPTER NUMBER
Chapter 3
Chapter 4
Chapter 5
Index
REVISION
NUMBER
Rev. 9
Rev. 9
Rev. 9
Rev. 9
i-1

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