CERTIFICATION
Caution
This device has been tested and found to comply with the emissions
requirements of IEC 60601-1-2:2001-09. These requirements provide
reasonable protection against harmful electromagnetic interference in
a typical medical installation. However, high levels of radio-frequency
emissions from electrical devices, such as cellular phones, may disrupt
the performance of this device. To mitigate disruptive electromagnetic
interference, position this device away from radio frequency transmitters
and other sources of electromagnetic energy.
12
CERTIFICATION
This Dental Equipment is CE certified for Europe as a class 2a medical
device under the European Medical Device Directive 93/42/EEC. The
product complies with standards; Europe: IEC 60601-1, Canada: CAN/
CSA-C22.2 No. 601.1 and USA: UL 60601-1. It has also been certified to
latest medical device safety standards of *IEC 60601-1, as well as IEC
80601-2-60 for Dental Equipment.
Note
Testing included the latest versions of this standard for the United States
and Canada.
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