Gastrointestinal catheter/endoscope tracking system sensor, body-surface - UK MHRA Medical Device Registration

Gastrointestinal catheter/endoscope tracking system sensor, body-surface is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 108902. The device is manufactured by FUJIFILM Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Fujifilm Healthcare UK Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Gastrointestinal catheter/endoscope tracking system sensor, body-surface

MHRA Device ID: 108902•Ref: 108902

Device Type

General Medical Device

Devices

Gastrointestinal catheter/endoscope tracking system sensor, body-surface

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 16, 2024

Manufacturer Information

Name

FUJIFILM Corporation

Address

26-30 Nishiazabu 2-chome Minato-ku 26-30

Tokyo, Japan

Created Date

Oct 18, 2021

Authorized Representative

Name

Fujifilm Healthcare UK Limited

Relationship Type

UK Responsible Person

Address

Fujifilm House Whitbread Way

Bedford, England, United Kingdom

Postcode: MK42 0ZE

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Other Products from FUJIFILM Corporation (10)

Other Products from Same Authorized Representative (10)

Gastrointestinal catheter/endoscope tracking system sensor, body-surface - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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