Satelec Mini LED Autofocus, User Manual

Page: 14 / 80

13 - 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 17),
for information on how to proceed.
14 – 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 other than those supplied by SATELEC have
been used;
- the instructions in this document have not been
followed.
The manufacturer reserves the right to modify the unit
and/or the Operating Manual without notice.
15 - 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 ISO 13485-certified quality assurance
system.
16 – SYMBOLS AND ABBREVIATIONS
Note:
Technical personnel of the Satelec authorized dealer
network can obtain from
ACTEON Group on request all
the information they need for repair of the parts of the
curing light that ACTEON has identified as repairable.
14
SYMBOL DEFINITION
Alternating current
Direct current
Warning, please refer to the
accompanying documentation
Class 2M laser
Type B
Class 2
H02926.S3.V4.qxp 13/03/2008 11:07 Page 14