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.
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Manufacturer's By Device Gastrointestinal catheter/endoscope tracking system sensor body-surface-Gastrointestinal catheter/endoscope tracking system sensor body-surface
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
FUJIFILM Corporation
26-30 Nishiazabu 2-chome
Minato-ku 26-30
Tokyo
106-8620
Japan
Fujifilm UK Limited
Fujifilm House Whitbread Way
Bedford
MK42 0ZE
England United Kingdom
04/12/2022
19437
FUJIFILM Corporation
26-30 Nishiazabu 2-chome
Minato-ku 26-30
Tokyo
106-8620
Japan
Fujifilm UK Limited
Fujifilm House Whitbread Way
Bedford
MK42 0ZE
England United Kingdom
04/12/2022
19577