GE LOGIQ E9 Service Manual

GE
D
IRECTION 5535208-100, REV. 2 LOGIQ E9 SERVICE MANUAL
1 - 10 Section 1-3 - Important conventions
This unit carries the CE mark.
The LOGIQ E9 unit complies with
regulatory requirements of the
European Directive 93/ 42/EEC
concerning medical devices.
It also complies with emission limits for
a Group 1, Class B Medical Device as
stated in EN 60601-1-2
(IEC 60601-1-2).
Rear of console
“CAUTION” The equilateral triangle is
usually used in combination with other
symbols to advise or warn the user.
Various
Shear Wave Option Capacitor Pack
“ATTENTION - Consult
accompanying documents”
is intended to alert the user to refer to
the operator manual or other
instructions when complete information
cannot be provided on the label.
General Warning
Various,
Rear Cover,
Probe Label
“Warning - Dangerous Voltage”
(the lightning flash with arrowhead in
equilateral triangle) is used to indicate
electric shock hazards.
Various
“Mains OFF”
Indicates the power off position of the
mains power switch.
Rear of system adjacent to
MAINS Switch
Table 1-6 Product icons (Continued) 3 of 7
LABEL/SYMBOL PURPOSE/MEANING LOCATION

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