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 - Rudy Project S.p.A.

Address:

Via B. Marcello 44

Treviso

TV 31100

Italy

Authorised Representative/ UK Responsible Person
Name: Donawa Lifescience Ltd
Address:

Aviation Business Park Enterprise Close

Christchurch

BH23 6NX

England United Kingdom

Code/Term Type

Spectacle frame Spectacle frame Class I

Prescription spectacle lens custom-made Prescription spectacle lens custom-made 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 custom-made	Prescription spectacle lens custom-made	Class I