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 - Safilo S.p.A.

Address:

Via Settima Strada n. 15

Padova

35129

Italy

Authorised Representative/ UK Responsible Person
Name: Safilo UK Ltd.
Address:

Savoy Hill House 7-10 Savoy Hill

London

WC2R 0BU

England United Kingdom

Code/Term Type

Prescription spectacles Prescription spectacles 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
Prescription spectacles	Prescription spectacles	Class I
Spectacle frame	Spectacle frame	Class I