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Version 22.03
Manufacturer contact details
Conformity
Van Raam declares as manufacturer that the tricycles, as described in this manual, are
produced in accordance with the Medical Devices Regulation (EU) 2017/745, risk category
1. All products have been produced in accordance with the 2006/42/EG guidelines. The
signed declaration of conformity can be found on the Van Raam website.
Introduction
This user manual provides important and necessary
information about the use of your tricycle. We ask you to read
this manual thoroughly before using the tricycle. Always follow
the instructions as provided in this user manual and keep the
manual carefully. The most current version of the user manual
can be found on the product page of the bicycle on the website
All safety and user aspects have to be made clear to children
and to people with limited powers of perception by a
responsible and supervising person.
+31 (0)315
–
25 73 70
[email protected]
www.vanraam.com
Van Raam
Guldenweg 23
7051 HT Varsseveld, The Netherlands
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