Disposal And Recycling; Manufacturer's Liability; Regulations; Symbols - Satelec Acteon P MAX Newtron XS Manual De Instrucciones

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 23/01/2003).
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
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 93/42/EEC.
This equipment is manufactured in compliance
with the current IEC 60601-1 standard.
This equipment has been designed and
manufactured according to an EN ISO 13485-
certified quality assurance system.
XIV - SYMBOLS
installation
Alternating current
BF device
Warning, please refer to the
accompanying documentation
Not to be disposed of as household
waste
CE Marking
Tank selection
Air function
Flush
Irrigation
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