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

Back to MHRA

Manufacturer's Devices - Bonalive Biomaterials ltd

Address:

Biolinja 12

Turku

FI-20750

Finland

Authorised Representative/ UK Responsible Person
Name: Neptune Medical Limited
Address:

2 Forest Farm Business Park

York

YO19 4RH

United Kingdom

Code/Term Type

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

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.