W&H Implantmed, Инструкция по эксплуатации

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10
Introduction
Production according to EU Directive
The medical device complies with the regulations of Directive 93/42/EEC.
Responsibility of the manufacturer
The manufacturer can only accept responsibility for the safety, reliability and performance of the Implantmed
when compliance with the following instructions is ensured:
> The Implantmed must be used in accordance with these Instructions for Use.
> The Implantmed has no components that can be repaired by the user.
> Modifications or repairs must only be undertaken by an authorized W&H service partner (see page 62).
> The electrical installation at the premises must comply with the regulations laid out in IEC 60364-7-710
(“Installation of electrical equipment in rooms used for medical purposes”) or with the regulations applicable in your country.
> Unauthorized opening of the control unit invalidates all claims under warranty and any other claims.
In addition to unauthorized assembly, installation, modification of or repairs to the control unit, motor with cable,
transmission instrument and non-compliance with our instructions, improper use will void the warranty and release us
from all other claims.