DKL L2-S300, Operating Instructions Manual, Page: 168 / 327

9
Introduction
Hereby, W&H declares that the medical product is in compliance with Directive 2014/53/EU (RED).
The full text of the EU declaration of conformity is available at the following internet address https://wh.com
Responsibility of the manufacturer
The manufacturer can only accept responsibility for the safety, reliability and performance of the foot control when 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 respective foot control may only be used with the control unit listed in the scope of delivery.
Improper use, unauthorized assembly, modification or repair to the medical device, non-compliance with our instructions or the use
of accessories and spare parts which are not approved by W&H, invalidates all claims under warranty and any other claims.
Any serious incident that has occurred in relation to the medical device should be reported to the manufacturer and the
competent authority!