GE H
EALTHCARE
D
IRECTION
GA091568, R
EVISION
5
VIVID E9 S
ERVICE
M
ANUAL
Chapter 1 - Introduction
1 - 27
VIVID E9
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”
GOST
This symbol indicates that waste electrical and
electronic equipment must not be disposed of as
unsorted municipal waste and must be collected
separately. Please contact an authorized
representative of the manufacturer for information
concerning the decommissioning of your equipment.
This unit carries the CE mark.
The VIVID 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).
GROUP 1 Class A
(Some units produced in 2010 are Class B).
Table 1-17 Label on Rear Cover - detailed descriptions (cont’d) sheet 2 of 3
DESCRIPTION
ILLUSTRATION
Содержание Vivid E9
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