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 - Central Lab VE Limited

Address:

Unit 3 Linkme 1 Close Queens Drive Industrial Estate

Nottingham

NG2 1NA

United Kingdom

Serilization:

Authorised Representative
Name: Not Available

Address:

Code/Term Type

Spectacle Lenses Class I

Prescribed Spectacles

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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