GE Medical Systems
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 7. It applies to all versions of the R3.0.2
software for the LOGIQ 7 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: 49 212.28.02.431
Beethovenstraße 239
Postfach 11 05 60
D-42655 Solingen
GERMANY
Summary of Contents for LOGIQ 7
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Page 16: ...i 14 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 28: ...Introduction 1 12 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 140: ...Preparing for an Exam 4 28 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 306: ...Scanning Display Functions 6 42 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 418: ...Abdomen and Small Parts 8 18 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 644: ...Cardiology 10 128 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 688: ...Urology 12 8 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 698: ...Pediatrics 13 10 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 882: ...Customizing Your System 16 106 LOGIQ 7 Basic User Manual Direction 2392206 100 Rev 1 ...
Page 928: ...Probes and Biopsy 17 46 LOGIQ 7 Online Help Direction 2392536 100 Rev 1 ...
Page 974: ...User Maintenance 18 46 LOGIQ 7 Online Help Direction 2392536 100 Rev 1 ...
Page 983: ...GE Medical Systems ...
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