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Direction 2406547-100
Rev. 0
0459
Regulatory Requirement
This product complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices.
0459
This manual is a reference for the LOGIQ 3. It applies to all versions of the >=R2.0.0 software for the LOGIQ 3 ultrasound system.
GE Medical 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: 49 212.28.02.207 Deutschland GmbH & Co. KG: FAX: 49 212.28.02.431 Beethovenstrae 239 Postfach 11 05 60 D-42655 Solingen GERMANY
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