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 - LUXOTTICA GROUP S.p.A.

Address:

Piazzale Cadorna 3

Milano

20123

Italy

Authorised Representative/ UK Responsible Person
Name: LUXOTTICA NORTH EUROPE Ltd
Address:

Level 2 The Kensington Building

1 Wrights Lane

London

W8 5RY

England United Kingdom

Code/Term Type

Spectacle frame Spectacle frame Class I

Prescription spectacle lens non-customized Prescription spectacle lens non-customized Class I

Tinted spectacle lens prescription standard Tinted spectacle lens prescription standard Class I

Tinted spectacle lens prescription standard Tinted spectacle lens prescription standard 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
Spectacle frame	Spectacle frame	Class I
Prescription spectacle lens non-customized	Prescription spectacle lens non-customized	Class I
Tinted spectacle lens prescription standard	Tinted spectacle lens prescription standard	Class I
Tinted spectacle lens prescription standard	Tinted spectacle lens prescription standard	Class I