Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Blumil Milosz Krawczyk

Address:

Ul. Giedowa 4B/11 Warszawa

Warszawa

Mazowieckie 01-211

Poland

Authorised Representative/ UK Responsible Person
Name: Ride LEV Limited
Address:

85 Great Portland Street

London

London

W1W 7LT

England United Kingdom

Code/Term Type

Wheelchair electric-motor-driven propulsion system Wheelchair electric-motor-driven propulsion system Class I

Wheelchair electric-motor-driven propulsion system Wheelchair electric-motor-driven propulsion system Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Wheelchair electric-motor-driven propulsion system	Wheelchair electric-motor-driven propulsion system	Class I
Wheelchair electric-motor-driven propulsion system	Wheelchair electric-motor-driven propulsion system	Class I