Faro DKL L2-ECO Notice D'utilisation page 58

Qualifications of the user
We have based our development and design of the medical device on the dentists, dental hygienists, dental
employees (prophylaxis) and dental assistants target group.
Production according to EU Directive
The medical device meets the requirements of Directive 93/42/EEC.
Responsibility of the manufacturer
The manufacturer can only accept responsibility for the safety, reliability and performance of the medical device
when it is used in compliance with the following directions:
> The medical device and the supply hose must be used in accordance with these Instructions for use.
> The medical device and the supply hose has no components that can be repaired by the user. Assembly,
modifications or repairs must only be undertaken by an authorized W&H service partner (see page 44).
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