Acteon SOPROCARE User Manual page 9

E N G L I S H
4.3. MEDICAL DEVICE VIGILANCE
As with any medical device, this device is subjected to medical device vigilance dispositions; any serious dysfunction should then be
the subject of a description to the competent authorities and to the manufacturer as soon as possible and as precisely as possible.
4.4. END OF LIFE
This device bears the recycling symbol according to the European directive 2002/96/EC about electric and electronic equipment
waste (DEEE or WEEE). By correctly disposing of this device, you will contribute to avoiding any damage to the environment and
human health.
The symbol on the device or on the accompanying documentation indicates this product cannot be, in any case, treated as
household waste. Therefore, it should be transferred to a waste collection centre that handles electric and electronic equipment
recycling. Please respect the standards relative to waste disposal in force in the installation country. For more details about the
device treatment, recuperation and recycling, please contact your dental device distributor (or failing that, the group ACTEON site
www.acteongroup.com), so that you can be informed of the procedure.
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SOPROCARE • User's manual