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 - Inami & Co. Ltd.

Address:

No 24-2 Hongo 3-Chome Bunkyo-Ku

Tokyo

113-0033

Japan

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

Perimeter manual Perimeter manual Class I

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

Trial lens frame Trial lens frame Class I

Ophthalmic tonometer line-powered Ophthalmic tonometer line-powered 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
Perimeter manual	Perimeter manual	Class I
Vision testing/training chart	Vision testing/training chart	Class I
Trial lens frame	Trial lens frame	Class I
Ophthalmic tonometer line-powered	Ophthalmic tonometer line-powered	Class I