GE Healthcare

LOGIQ E10s Basic User Manual Rev 3 March 2020

Basic User Manual

1470 Pages

Revision History Reason for Change DATE (YYYY/MM/DD)  REV  REASON FOR CHANGE  Rev. 1  2019/12/06  Initial release  Rev. 2  2019/12/20  Update Chapter 2 Device label, Warning for effects from cauterizing knife and Color Flow Doppler.  Rev. 3  2020/03/31  Update Indication for Use in Chapter 2.  List of Effective Pages  PAGE NUMBER  REVISION NUMBER  PAGE NUMBER  REVISION NUMBER  Title Page  Rev. 3  Chapter 6  Rev. 3  Revision History  Rev. 3  Chapter 7  Rev. 3  Regulatory Requirements  Rev. 3  Chapter 8  Rev. 3  Table of Contents  Rev. 3  Chapter 9  Rev. 3  Chapter 1  Rev. 3  Chapter 10  Rev. 3  Chapter 2  Rev. 3  Chapter 11  Rev. 3  Chapter 3  Rev. 3  Chapter 12  Rev. 3  Chapter 4  Rev. 3  Chapter 13  Rev. 3  Chapter 5  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 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 E10s – Basic User Manual Direction 5807721-1EN Rev. 3  i-1
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