Safety and Maintenance
14.1 Safety
13
Page 27
The en
Puls
Version 2.0 is manufactured in accordance with the
DIN EN 60601-1 safety regulations.
Zimmer MedizinSysteme GmbH shall only be held responsible for the 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,
•
extensions, readjustments, or modifications are only performed by persons
authorized by Zimmer MedizinSysteme GmbH,
•
the user has been instructed in the functional safety, proper operating
condition, and the 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 immediately disconnected from the power supply upon the
penetration of liquid.
The device contains no parts that can be maintained or repaired by the
operator.
Modification of this device is not permitted.
Service and replacement of components may only be performed by certified
service technicians from Zimmer MedizinSysteme GmbH.
