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 - FE-Group S.r.l

Address:

Viale Dell' Industria 42 21052 Busto Arsizio

VA Italy

21052

Italy

Authorised Representative/ UK Responsible Person
Name: Grafton Optical Company Limited
Address:

Unit 7 River Park Industrial Estate Billet Lane

Berkhamsted

Hertfordshire HP41HL

England United Kingdom

Code/Term Type

Ophthalmic tonometer probe Ophthalmic tonometer probe Class I

Diagnostic ophthalmic prism Diagnostic ophthalmic prism 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
Ophthalmic tonometer probe	Ophthalmic tonometer probe	Class I
Diagnostic ophthalmic prism	Diagnostic ophthalmic prism	Class I