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Regulatory Requirement
LOGIQ 7/LOGIQ 7 Pro complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices.
This manual is a reference for the LOGIQ 7/LOGIQ 7 Pro. It applies to all versions of the R8.x.x software and later for the LOGIQ 7/LOGIQ 7 Pro
ultrasound systems.
Manufacturer
GE-Yokogawa Medical Systems, Ltd.
7-127 Asahigaoka 4-Chome, Hino-shi
Tokyo, 191-8503
JAPAN
Country-specific
MHLW: 21300BZZ00082000
SFDA REG. No: (I) 20073230515 / YZP/JAP 0004-2006
GE Medical System: 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 Healthcare
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