Disposal And Recycling - Satelec P5 Newtron XS Gebrauchsanleitung

XI - -DISPOSAL AND RECYCLING
As electrical and electronic equipment, the device must be disposed of according to a specialized
procedure for collection, pick-up and recycling or destruction (in particular on the European market,
with reference to Directive 2002/96/EC of 27/01/2003).
When your device reaches the end of its life, we consequently recommend that you contact your dental
equipment dealer (or, failing this, the nearest ACTEON GROUP office, the list of which is given in
chapter 15), for information on how to proceed.
XII - -LIABILITY
The manufacturer is not liable if:
- the manufacturer's installation recommendations have not been followed (supply voltage,
electromagnetic environment, etc.),
- repairs have been performed by persons not authorized by the manufacturer,
- the device has been used in an electrical installation which does not comply with current standards,
- the device has been used in a way which is not stipulated in this manual,
- accessories (tips, handpiece, pump, etc.) other than those supplied by SATELEC have been used,
- the instructions in this document have not been followed.
Note:
The manufacturer reserves the right to modify the device and/or the user manual without notice.
XIII - REGULATIONS
This medical device is classified as class IIa according to European Directive relevant to Medical Devices
currently in force.
This equipment is manufactured in compliance with the current IEC 60601-1 standard.
This equipment has been designed and manufactured according to an ISO 13485-certified quality
assurance system.