KLICK devices - End User’s Manual (EN) - rev.7.2 of 2021.11.25
Dear customer,
Thank you for choosing a KLICK product.
We sincerely hope that the KLAXON MOBILITY products can improve your day and your activities in many ways
and we remain at your disposal for any information or clarification you may require. We also encourage you to keep
up to date on the latest news of our product range, on the accessories available and on our company’s events and
initiatives.
You can contact us by writing an e-mail to info@klaxon-klick.com, through our web site at www.klaxon-klick.com,
on our Linkedin page www.linkedin.com/company/klaxon-mobility or on our Facebook page www.facebook.com/
klaxonklickworld.
Please note also that in compliance with European regulation, KLAXON MOBILITY GMBH holds CE
certification for all the products in the KLICK range; they are classified as Class I medical devices
according to Annex VIII EU745/2017 MDR and they comply with the essential requirements of Annex
I EU745/2017 MDR and Annex I of the European Medical Devices Directive 93/42/EEC, as modified
by the Directive 07/47/EEC.
KLICK devices belongs to:
- GMDN 42805 code (Wheelchair electric-motor-driven propulsion system)
- UMDNS 17952 code (Power Conversion Kits, Wheelchair)
EU WARNING: In the event of any serious accident related to the KLICK device, the user must
immediately notify the manufacturer and the competent authority of the European country where
the user has bought the product.
NOTE
For visually impaired people, a pdf format of this manual is available on our website www.klaxon-
klick.com.
NOTE
You can find the addresses of Klaxon Dealers on our website www.klaxon-klick.com in the “Klick
Stores” area.
Thank you again for having chosen our products. We wish you a good day and enjoyable use.
Best regards,
The Staff of KLAXON MOBILITY GMBH
KLAXON Mobility GmbH - EN
To Next Page
