GE LOGIQ V1 User Manual

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 V2, LOGIQ V1. It applies to all versions of
the R1.x.x for the LOGIQ V2/LOGIQ V1 ultrasound system.
GE
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

GE LOGIQ V1 Specifications

General

Brand	GE
Model	LOGIQ V1
Category	Medical Equipment
Language	English