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 - WENZHOU MINGSHIDA LIGHT INDUSTRIAL PRODUCTS CO. LTD.

Address:

No.55 HaoXiang Road Louqiao Residential Quarter Ouhai

Wenzhou

ZheJiang 325006

China

Authorised Representative/ UK Responsible Person
Name: KINGSMEAD SERVICE LIMITED
Address:

19 MEZZANINE FLOOR 19-21 CRAWFORD STREET

London

W1H 1PJ

England United Kingdom

Code/Term Type

Pre-prescription spectacle lens Pre-prescription spectacle lens Class I

Spectacle frame Spectacle frame Class I

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
Pre-prescription spectacle lens	Pre-prescription spectacle lens	Class I
Spectacle frame	Spectacle frame	Class I