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GE Logiq 9 User Manual

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    Page 1 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
    Page 2 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...
    Page 3 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....
    Page 4 i-2 LOGIQ E9 User Guide Direction 5180302-100 Rev. 1 This page intentionally left blank.
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