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Beschikbare talen
Beschikbare talen
The CE mark on the device confirms conformity with the European
requirements of the Medical Device Regulation (2017 / 745 / EU
Medical Device Directive (MDR)).
- 2011 / 65 / EC + 2015 / 863 / EC RoHS-Directive
- 2012 / 19 / EC WEEE-Directive
- 2014 / 53 / EC RED-Directive
Complete declarations of conformity are availa-
ble on the Internet at www.humantechnik.com
in the service area.
All serious incidents must be reported to
the manufacturer and the according local
authority!
Humantechnik's UK authorised representative:
Sarabec Ltd., hereby declares that this device
complies with all UK statutory instruments.
UK declaration of conformity available from:
Sarabec Ltd.
Sarabec Ltd.
15 High Force Road
MIDDLESBROUGH TS2 1RH
United Kingdom
English 45
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