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 - Osteopore International Pte Ltd

Address:

2 Tukang Innovation Grove #09-06/07

JTC MedTech Hub

618305

Singapore

Authorised Representative/ UK Responsible Person
Name: Easy Medical Device Limited
Address:

125 Deansgate

Manchester

M3 2LH

Wales United Kingdom

Code/Term Type

Bone matrix implant synthetic non-antimicrobial Bone matrix implant synthetic non-antimicrobial Conformity Assessment Certificate Expired Class III

Bone matrix implant synthetic non-antimicrobial Bone matrix implant synthetic non-antimicrobial

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 Conformity Assessment Certificate Expired	Class III
Bone matrix implant synthetic non-antimicrobial	Bone matrix implant synthetic non-antimicrobial