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 - Zhejiang Jingjia Medical Technology Co. Ltd.

Address:

Room 301-318 Floor 3 Building 2 and Room 105 Floor 1 Room 201 Floor 2 and Floor 3 Building 3 206# Zhenzhong Road

Sandun Town Xihu District

Hangzhou Zhejiang

310030

China

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

Subconjunctival bleb space-occupying material Subconjunctival bleb space-occupying material Class IIb

Cartilage biomatrix implant human-derived Cartilage biomatrix implant human-derived Class III

Joint lubrication gel Joint lubrication gel 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
Subconjunctival bleb space-occupying material	Subconjunctival bleb space-occupying material	Class IIb
Cartilage biomatrix implant human-derived	Cartilage biomatrix implant human-derived	Class III
Joint lubrication gel	Joint lubrication gel	Class III