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 - Cristalens Industrie

Address:

4 Rue Louis De Broglie

Lannion

22300

France

Authorised Representative/ UK Responsible Person
Name: Vision Matrix Ltd
Address:

Vision Matrix Ltd 31 East Parade

Harrogate

North Yorkshire HG1 5LQ

England United Kingdom

Code/Term Type

Posterior-chamber intraocular lens pseudophakic Posterior-chamber intraocular lens pseudophakic Class IIb

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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