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 - Motek Medical B.V.

Address:

Vleugelboot 14 3991 CL

Houten

Netherlands

Authorised Representative/ UK Responsible Person
Name: Brighthedge Ltd T/A Summit Medical and Scientific
Address:

12 Swanns Meadow Bookham

Leatherhead

Surrey KT23 4jX

England United Kingdom

Code/Term Type

Gait rehabilitation frame electric Gait rehabilitation frame electric

Lower limb sliding exerciser powered Lower limb sliding exerciser powered Class I

Physical therapy table line-powered Physical therapy table line-powered Class I

Treadmill/elliptical gait rehabilitation system Treadmill/elliptical gait rehabilitation 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
Gait rehabilitation frame electric	Gait rehabilitation frame electric
Lower limb sliding exerciser powered	Lower limb sliding exerciser powered	Class I
Physical therapy table line-powered	Physical therapy table line-powered	Class I
Treadmill/elliptical gait rehabilitation system	Treadmill/elliptical gait rehabilitation system	Class I