Satelec IMPLANT CENTER 2 User Manual page 31

13. 5 CABLE LENGTHS
Cables and accessories Maximum length
Handpiece cords
Footswitch cord
Power supply cord
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 followed (supply voltage,
electromagnetic environment, etc.)
RF emission, CISPR 1 - Class A/Group 1
Harmonic current emission: IEC61000-3-2
Voltage fluctuation: IEC61000-3-3
Immunity to electrostatic discharge: IEC61000-4-2
Immunity to electrical fast transients/bursts: IEC61000-4-4
Less than 3m
Immunity to surges: IEC61000-4-5
Immunity to voltage dips, short interruptions and voltage variations:
IEC61000-4-11
Immunity to conducted disturbances induced by radiofrequency fields: IEC61000-4-6
Immunity to radiated radiofrequency electromagnetic fields: IEC61000-4-3
Complies with:
- 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 specified 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.
XVI - 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.
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