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

Back to MHRA

Manufacturer's Devices - FUJIFILM Corporation

Address:

26-30 Nishiazabu 2-chome

Minato-ku 26-30

Tokyo

106-8620

Japan

Authorised Representative/ UK Responsible Person
Name: Fujifilm UK Limited
Address:

Fujifilm House Whitbread Way

Bedford

MK42 0ZE

England United Kingdom

Code/Term Type

Flexible video colonoscope reusable Flexible video colonoscope reusable Class IIa

Gastrointestinal catheter/endoscope tracking system sensor body-surface Gastrointestinal catheter/endoscope tracking system sensor body-surface Class I

Mobile medical equipment stand non-powered Mobile medical equipment stand non-powered Class I

Electromagnetic endoscope tracking system image processing unit Electromagnetic endoscope tracking system image processing unit Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Flexible video colonoscope reusable	Flexible video colonoscope reusable	Class IIa
Gastrointestinal catheter/endoscope tracking system sensor body-surface	Gastrointestinal catheter/endoscope tracking system sensor body-surface	Class I
Mobile medical equipment stand non-powered	Mobile medical equipment stand non-powered	Class I
Electromagnetic endoscope tracking system image processing unit	Electromagnetic endoscope tracking system image processing unit	Class IIa