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 - Kay Pictures Ltd

Address:

Unit 39 Silk Mill Business Park Brook Street

Tring

Herts HP23 5EF

United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Vision/eye movement analysis system Vision/eye movement analysis system Class I

Eye patch Eye patch Class I

Vision testing/training chart Vision testing/training chart Class I

Spectacle lens foil Spectacle lens foil Class I

Ocular occluder/Maddox rod Ocular occluder/Maddox rod Class I

Vision testing/training flipper Vision testing/training flipper 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
Vision/eye movement analysis system	Vision/eye movement analysis system	Class I
Eye patch	Eye patch	Class I
Vision testing/training chart	Vision testing/training chart	Class I
Spectacle lens foil	Spectacle lens foil	Class I
Ocular occluder/Maddox rod	Ocular occluder/Maddox rod	Class I
Vision testing/training flipper	Vision testing/training flipper	Class I
Diagnostic ophthalmic prism	Diagnostic ophthalmic prism	Class I