GE HEALTHCARE
DIRECTION FC091194, REVISION 11 VIVID 7 SERVICE MANUAL
1 - 46 Section 1-5 - Labels Locations
Vivid 7 SCANNERS PRODUCED
AFTER SEPTEMBER 2004:
“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”
Products produced before September
2004 will bear the c-UL-us Classification
mark, shown below.
Vivid 7 SCANNERS PRODUCED AFTER SEPTEMBER 2004:
Vivid 7 SCANNERS PRODUCED
BEFORE SEPTEMBER 2004:
“CLASSIFIED BY UNDERWRITERS
LABORATARIES INC WITH RESPECT
TO ELECTRICAL SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN
ACCORDANCE WITH UL2601-1 AND
CAN/CSA C22.2 NO.601.1”
This unit carries the CE mark.
The Vivid 7 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).
(Units produced before 2 May 2002
have the CE0301 label.)
The sign indicates that Non Ionizing
Radiation is/may be emitted from the
unit.
Table 1-23 Label on Rear Cover - Vivid 7, Details Descriptions (cont’d) sheet 2 of 2
DESCRIPTION ILLUSTRATION
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