RSR-000886-000 (1)
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Cet équipement est conforme aux limites d’exposition aux rayonnements ISED établies
pour un environnement non contrôlé. Cet équipement doit être installé et utilisé à plus de
20 cm entre le radiateur et votre corps.
7.6. Radio Equipment Directive (RED)
The device is SAR exempt based on the operation of the device being under the SAR
exemption requirements.
7.7. Disposal
If you plan to discontinue the use of this laser system, and intend to dispose of
it or any of its parts or accessories, you must observe the applicable regional
legal provisions for its disposal. You may also contact your local distributor,
authorized service center, or Customer Care for the disposal options for this
laser system.
8. Labeling
8.1. Explanation of Symbols
Symbol
Title
Description
Manufacturer
Indicates the medical device manufacturer, as
defined in EU Directives 90/386/EEC, 93/42/EEC
and 98/79/EC.
Date of manufacture
Indicates the date when the medical device was
manufactured.
Catalog number
Indicates the manufacturer’s catalog, or model,
number so that the medical device can be identified.
Serial number
Indicates the manufacturer’s serial number so that a
specific medical device can be identified.
Caution
Indicates the need for the user to consult the
instructions for use for important cautionary
information such as warnings and precautions that
cannot, for a variety of reasons, be presented on the
medical device itself.
Type B Applied Part
Refers to the part of the medical device which comes
into physical contact with the patient in order for the
device to carry out its intended function.
