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 - Canon Inc.

Address:

9-1 Imaikami-cho Nakahara-ku

Kanagawa

211-8501 Kawasaki

Japan

Authorised Representative/ UK Responsible Person
Name: Canon (UK) Ltd
Address:

4 Roundwood Avenue Stockley Park

Uxbridge

UB11 1AF

England United Kingdom

Code/Term Type

Computed radiography digital imaging scanner Computed radiography digital imaging scanner Class IIa

Retinal optical coherence tomography system Retinal optical coherence tomography system Class IIa

Posterior eye segment analyser software Posterior eye segment analyser software Class IIa

Ophthalmic tonometer line-powered Ophthalmic tonometer line-powered Class IIa

Ophthalmic fundus camera Ophthalmic fundus camera Class I

Automated ophthalmic refractometer Automated ophthalmic refractometer 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
Computed radiography digital imaging scanner	Computed radiography digital imaging scanner	Class IIa
Retinal optical coherence tomography system	Retinal optical coherence tomography system	Class IIa
Posterior eye segment analyser software	Posterior eye segment analyser software	Class IIa
Ophthalmic tonometer line-powered	Ophthalmic tonometer line-powered	Class IIa
Ophthalmic fundus camera	Ophthalmic fundus camera	Class I
Automated ophthalmic refractometer	Automated ophthalmic refractometer	Class I