Zimmer Z Wave Q, User Manual

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Safety and Maintenance
13
Page 17
The ZWave
Q
is manufactured according to the IEC 60601-1 safety regulations.
a) Zimmer MedizinSysteme GmbH can only be held responsible for safety and
reliability of the device if

the device is operated using a proper power outlet with earth contact and the
electrical installation complies with DIN VDE 0100 part 710,

the device is operated in accordance with the operating instructions,

extentions, readjustments or modifications are only performed by persons
authorised by Zimmer MedizinSysteme GmbH,

the user has been instructed in the functional safety, proper operating
condition, and mechanical integrity of the device and handpiece prior to use,

the device is only operated by properly trained personnel,

the device is not operated in hazardous areas and/or a combustive
atmosphere,

the device is disconnected immediately from the power supply upon the
penetration of liquid.
b) The device contains no parts that can be maintained or repaired by the operator.
c) The device does not contain any parts that can be serviced and repaired by the
operator.
d) Fuses and other spare parts may only be replaced by trained service personnel.
e) Replacement of the lithium battery by untrained personnel may result a hazard.
f) The device may only be serviced by trained personnel.
g) Required service can be found in the Service Manual
ZWave
Q
or can be obtained
from the manufacturer.
h) Zimmer MedizinSysteme GmbH will provide circuit diagrams, component lists,
descriptions, calibration instructions or other documents on request.
Legal Notice For installation and operation of this equipment, national laws must be observed.