Regulatory Requirement
LOGIQ E9 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 Version R4 software for
the LOGIQ E9 ultrasound system.
GE Healthcare
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)
GE Ultraschall Deutschland GmbH & Co. KG
Beethovenstrasse 239
Postfach 11 05 60
D-42655 Solingen GERMANY
TEL: 49 212.28.02.208; FAX: 49 212.28.02.431
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