GE
D
IRECTION GB091046, REVISION 2 VIVID E9 / VIVID E7 BT’13 SERVICE MANUAL
Chapter 1 - Introduction 1 - 9
The system is not designed for use with
flammable anesthetic gases.
Rear of console
VIVID E9 / VIVID E7 SCANNERS
VIVID E9 / VIVID E7 SCANNERS
“TESTED AND PRODUCTION
MONITORED BY TUV PRODUCT
SERVICE NRTL WITH RESPECT TO
ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL2601-1 AND
CAN/CSA C22.2 NO.601.1”
REAR OF CONSOLE ON VIVID E9 /
VIVID E7
(Introduced 1. January 2016.)
This unit carries the CE mark.
The VIVID E9 / VIVID E7 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
(Used before 1. January 2016.)
This unit carries the CE mark.
The VIVID E9 / VIVID E7 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
“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.
VARIOUS
“CAUTION - Dangerous voltage”
(the lightning flash with arrowhead in
equilateral triangle) is used to indicate
electric shock hazards.
VARIOUS
Table 1-6 Product icons (cont’d) sheet 2 of 4
LABEL/SYMBOL PURPOSE/MEANING LOCATION
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