Trumpf TruSystem 7000, Руководство по обслуживанию

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Test procedures
Service Manual TruSystem 7000 Operating Table – 1 764 986 – 10/2016
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4 Test procedures
As the medical products from Trumpf Medical are distributed
worldwide, uniform guidelines for electrical retesting should be
used.
According to the IEC 60601-1 standard, the limit values according
to the CF classification apply when testing applied parts. Based on
the design type, the Trumpf Medical electric operating tables only
include one applied part of Class B .
Furthermore, the Trumpf Medical product-specific prescribed retests
and safety checks are obligatory.
All maintenance work must be carried out with the help of the
maintenance protocol and take into consideration the spare or
wearing parts list and the lubrication plan (see page 284).
Conduct a complete functional test after service work is completed.
Germany International
In Germany, initial testing and
retesting of electrical devices
are governed by the stipulations
of the accident prevention
regulation BGV A3 .
VDE 0751-1 is the standard that
serves as the basis for retesting
of electrical medical devices.
Therefore in accordance with
the VDE 0751-1 standard noted
above, the specifications based
on IEC 60601-1 are definitive
for Trumpf Medical medical
devices.
In countries with different
national legislation, the country-
specific standards and
guidelines for the retesting of
electrical medical devices are
mandatory.