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 - Ottobock SE & Co. KGaA

Address:

Max-Näder-Straße 15

Duderstadt

37115

Germany

Authorised Representative/ UK Responsible Person
Name: Otto Bock Healthcare PLC
Address:

32 Parsonage Road Englefield Green

Egham

Surrey TW20 0LD

United Kingdom

Code/Term Type

Hip orthosis Hip orthosis Class I

Knee support orthosis Knee support orthosis Class I

Ankle/foot orthosis Ankle/foot orthosis 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
Hip orthosis	Hip orthosis	Class I
Knee support orthosis	Knee support orthosis	Class I
Ankle/foot orthosis	Ankle/foot orthosis	Class I