NOVACARE 960800, Инструкция по эксплуатации

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20. Servicing/Maintenance
• The ProLift Cacero series is a medical product as defined by RL 93/42/EEC and the
Medical Devices Act (MPG) of the German Federal Republic, whose legal provisions
must be observed in their deployment and use.
• The system is suitable for sale or transfer elsewhere to be reused. Maintenance
requirements must, however, be observed and faultfree operation ensured.
• To ensure correct functioning of the ProLift Cacero, regular maintenance and safety
checks are required. These checks are separate from, and have no bearing on, the
safety checks, visual and functional tests and tests on maximum load using suitable
free-hanging reference weights as prescribed by law (in Germany, DGUV3).
• Maintenance and inspection must be carried out by the manufacturers or businesses
authorised by them and a charge will be made.
• If safety checks are not carried out, do not comply with the prescribed schedules or
technical specifications, or are not carried out by authorised persons, the warranties
will no longer be valid.
• Warranties will also be invalidated and liability denied in cases where damage or
functional failure for other reasons occur as a result of maintenance and inspection
not being carried out according to the specified schedules or technical specifications,
or of interference by unauthorised persons.
• Aside from those prescribed by law (in Germany, DGUV3) to be conducted by an
authorised person, the necessary checks and tests include
visual and functional tests (before use) by the user and
maximum load tests conducted by an authorised person
using suitable free-hanging reference weights.
• When the drive unit or CBJ is replaced, the maximum load
must be readjusted in order to establish the correct power
cut-off level for the entire new system.
Maintenance
should be
documented
on the service
labe