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 - Prosidyan Inc.

Address:

41 Spring St #107

New Providence

NJ 07974

United States

Authorised Representative/ UK Responsible Person
Name: Johnson & Johnson Medical Ltd
Address:

Baird House 4 Lower Gilmore Bank

Edinburgh

EH3 9QP

Scotland United Kingdom

Code/Term Type

Bone grafting cannula Bone grafting cannula Class IIa

Carbonic bone filling/substitute implant Carbonic bone filling/substitute implant 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 grafting cannula	Bone grafting cannula	Class IIa
Carbonic bone filling/substitute implant	Carbonic bone filling/substitute implant	Class III