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 - Nobles Medical Technologies II Inc.

Address:

17072 Newhope Street

Fountain Valley CA

92708

United States

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

Enterprise Hub NW Business Complex 1 Beraghmore Road

Derry Northern Ireland

BT48 8SE

Northern Ireland United Kingdom

Code/Term Type

Polyolefin/fluoropolymer suture monofilament Polyolefin/fluoropolymer suture monofilament 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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