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 - BAAT Medical Products B.V.

Address:

F. Hazemeijerstraat 800

Hengelo

Overijssel 7555 RJ

Netherlands

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Knee distraction orthosis Knee distraction orthosis Class I

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Class IIb

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
Knee distraction orthosis	Knee distraction orthosis	Class I
Metallic spinal interbody fusion cage	Metallic spinal interbody fusion cage	Class IIb