NOTE messages provide indications for easier maintenance and highlight important information.
1.1 MANUFACTURER RESPONSIBILITY
The manufacturer shall under no circumstances be held liable for injuries to persons or damage to property
caused by:
• Non-compliance with manufacturer recommendations during installation, whether this is the network voltage
or the electromagnetic environment,
• Maintenance or repair procedures performed by people who are unauthorized by the manufacturer,
• Use on an electrical xture that is not compliant with regulations in force,
• Uses other than those specied in this manual.
• Use of accessories (temple rest, chin rest, bites, etc.) other than those supplied by ACTEON Imaging,
• Use of hygienic protections different from class I Medical Device Directive 93/42/EEC and subsequent
amendments or not compliant with ISO 10993 series of standards.
• Non-compliance with the instructions contained in the accompanying documents.
Note: the manufacturer reserves the right to modify the medical device and/or any documentation without
notice.
1.2 WARRANTY
Any improper use or unauthorised modication to the medical device shall relieve the manufacturer of the
medical device, from the obligation to provide assistance covered by warranty and from any liability. This will
also result in additional charges for technical assistance not covered by warranty.
The warranty is valid only if the following requirements are complied with:
• Repairs, modications, adjustments and calibrations must be carried out solely by ACTEON Group or by qualied,
authorised and/or trained personnel.
• Installation must be carried out by qualied and trained technicians in compliance with the standards in force
and as recommend by the manufacturer.
• This medical device must be installed and used following the instructions provided in the installation manual
and in the attached documents.
• The mains power supply must provide the required power and its characteristics must meet the specications
indicated on the medical device identication label.
• The medical device must be periodically inspected by qualied, authorized and trained technical personnel in
compliance with the standards in force and with the manuals provided by the manufacturer.
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