Disposal And Recycling; Manufacturer'S Liability; Regulations - ACTEON Satelec Piezotome Solo Manual De Uso

XIV - 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 ACTEON Group
website, the address of which is given in chapter 18),
for information on how to proceed.
XV - MANUFACTURER'S
LIABILITY
The manufacturer is not liable if:
- the manufacturer's installation recommendations
have not been
electromagnetic environment, etc.)
- repairs or other work have been done on the device
by persons not authorized by the manufacturer
- the device has been used connected to an electrical
system that does not comply with current regulations
- the device has been used in ways other than those
speciÀ ed in this manual
- accessories (tips, handpiece, irrigation lines, 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's manual without notice.
followed (supply
XVI - REGULATIONS
This medical device is classiÀ ed 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-certiÀ ed quality assurance
system.
voltage,
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