GE HEALTHCARE
DIRECTION FC091194, REVISION 11 VIVID 7 SERVICE MANUAL
1 - 12 Section 1-3 - Important Conventions
Please refer to the Recycling
instructions on the label located outside
the Front End Card Rack’s Cover
(Inside the unit),
see Figure 1-20 on page 1-64
and Figure 1-23 on page 1-67.
REAR OF CONSOLE
Vivid 7 SCANNERS PRODUCED
AFTER SEPTEMBER 2004:
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.
REAR OF CONSOLE ON Vivid 7
PRODUCED AFTER SEPTEMBER
2004
Vivid 7 SCANNERS PRODUCED
BEFORE 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”
REAR OF CONSOLE ON Vivid 7
PRODUCED BEFORE SEPTEMBER
2004
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.)
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
Table 1-6 Product Icons (cont’d) sheet 2 of 4
LABEL/SYMBOL PURPOSE/MEANING LOCATION
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