GE Medical Systems LOGIQ 7 Reference Manual page 2

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 SW R3.0.0
and later software for the LOGIQ 7 ultrasound systems.
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
GE Medical Systems