GE LOGIQ E9 User Guide

LOGIQ E9 – User Guide i-3
Direction 5454884-100 English Rev. 1
Regulatory Requirements
Conformance Standards
The following classifications are in accordance with the IEC/
EN 60601-1:6.8.1:
• According to 93/42/EEC Medical Device Directive, this is
Class IIa Medical Device.
• According to IEC/EN 60601-1,
• Equipment is Class I, Type B with BF or CF Applied
Parts.
• According to CISPR 11,
• Equipment is Group 1, Class A ISM Equipment.
This product complies with the regulatory requirement of the
following:
• Council Directive 93/42/EEC concerning medical devices:
the CE label affixed to the product testifies compliance to
the Directive.
The location of the CE marking is shown in the Safety
chapter of this manual.
Authorized EU Representative
European registered place of business:
GE Medical Systems Information Technologies GmbH
(GEMS IT GmbH)
Munzinger Strasse 3, D-79111 Freiburg, GERMANY
Tel: +49 761 45 43 -0; Fax: +49 761 45 43 -233

GE LOGIQ E9 Specifications

General

Type	Ultrasound System
3D/4D Imaging	Yes
Transducer Ports	4 active ports
Connectivity	DICOM, USB, Ethernet
Applications	Abdominal, Vascular, Musculoskeletal, Small Parts, Urology, Pediatric, Cardiac, Obstetrics/Gynecology
Transducers	Linear, Convex, Phased Array, Volume
Doppler Modes	Color Doppler, Power Doppler, Pulsed Wave Doppler, Continuous Wave Doppler
Elastography	Yes
Advanced Features	B-Flow, Volume Navigation
Portability	Cart-based system
Display	19-inch high-resolution LCD monitor