5
Introduction
Production according to EU Directive
EU Directive 93/42/EEC has been used as a basis in the design and manufacture of this medical product and
this applies to the dental surgical units
– OSM2 SI-915 and
– OSM2 SI-923
in the condition as supplied by us. This declaration does not apply to non-specified fittings, mountings etc.
Responsibility of the manufacturer
The manufacturer can only accept responsibility for the safety, reliability and performance of the OSM2 when there
is compliance with the following directions:
– OSM2 must be used in accordance with these Instructions for Use.
– OSM2 has no components which can be repaired by the user. Assembly, modifications or repairs must only be
undertaken by skilled personnel authorized by W&H.
– The electrical installation at the premises must comply with the regulations of ÖVE-EN 7 ("Installation of
electrical equipment in rooms used for medical purposes") or with the regulations applicable in your country.
– Unauthorized opening of the equipment invalidates all claims under warranty and any other claims.
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