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Introduction
Production according to EU Directive
The foot control S-N1 and S-N2 is a medical device as defined by EU Directive 93/42/EEC.
The foot control S-NW is a medical device as defined by EU Directive 93/42/EEC and RED Directive 2014/53/EU.
Responsibility of the manufacturer
The manufacturer can only accept responsibility for the safety, reliability and performance of the foot control
if it is used in compliance with the following directions:
> The foot control must be used in accordance with these Instructions for Use and with the instructions
> for use of the drive unit.
> The foot control 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 31).
> Unauthorized opening of the foot control invalidates all claims under warranty and any other claims.
The foot control must be used only with the control unit listed in the equipment supplied.
In addition to unauthorized assembly, installation, modification of or repairs to the foot control or non-compliance
with our instructions, improper use will invalidate all claims made under warranty or otherwise.
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