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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 OPair, as described in this
user manual, is manufactured in accordance with Regulation (EU) 2017/745, risk class 1.
The OPair 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 OPair, 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 OPair 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 OPair 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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