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
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