Manufacturer Contact Details; Conformity Europe (Ce); Conformity Uk (Ukca) - Van Raam VeloPlus3 User Manual

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Delivery and service form .......................................................................................................................... 51

Manufacturer contact details

Van Raam
Guldenweg 23
7051 HT Varsseveld, The Netherlands
+31 (0)315 – 25 73 70
info@vanraam.com
www.vanraam.com

Conformity Europe (CE)

Van Raam Reha Bikes B.V., as manufacturer, declares that the VeloPlus3 as described in
this user manual is manufactured in accordance with Regulation (EU) 2017/745, risk class
1. The VeloPlus3 supplied with the Silent electrical system also complies with Directive
2006/42/EC including the applicable parts of EMC Directive 2014/30/EU and the NEN-EN
15194:2017 Bicycles - Electric supporting bicycles - EPAC Bicycles - part 4.2 Electrical
requirements. The signed declaration of conformity can be found on the Van Raam
website.

Conformity UK (UKCA)

Van Raam Reha Bikes B.V. as manufacturer declares that the VeloPlus3, as described in
this user manual, is manufactured in accordance with the "Essential Requirements of
Medical Devices Regulation 2002" (UK MDR 2002 Class 1 Medical Devices). The VeloPlus3
supplied with the Silent electrical system also complies with the "Machinery (Safety)
Directive SI 2008/1597" including the applicable parts of "Electro Magnetic Compatibility
Regulations SI 2016/1091" and the NEN-EN 15194:2017 Bicycles - Electric support
bicycles - EPAC Bicycles - part 4.2 Electrical requirements. The VeloPlus3 is provided with
UKCA label according to "EU Exit Regulations 2020/1478". The signed declaration of
conformity can be found on the Van Raam website.
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