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 - BONESUPPORT AB

Address:

Scheelevägen 19 Ideon Science Park

Lund

223 70

Sweden

Authorised Representative/ UK Responsible Person
Name: BONESUPPORT UK Ltd
Address:

Devonshire House 60 Goswell Road

London

EC1M 7AD

England United Kingdom

Code/Term Type

Bone matrix implant synthetic non-antimicrobial Bone matrix implant synthetic non-antimicrobial Class III

Bone matrix implant synthetic antimicrobial Bone matrix implant synthetic antimicrobial Class III

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
Bone matrix implant synthetic non-antimicrobial	Bone matrix implant synthetic non-antimicrobial	Class III
Bone matrix implant synthetic antimicrobial	Bone matrix implant synthetic antimicrobial	Class III