Endoscopic overtube, single-use - UK MHRA Medical Device Registration

Endoscopic overtube, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195118. 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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Endoscopic overtube, single-use

MHRA Device ID: 195118•Ref: 195118

Device Type

General Medical Device

Devices

Endoscopic overtube, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 20, 2024

Manufacturer Information

Name

FUJIFILM Corporation

Address

26-30 Nishiazabu 2-chome Minato-ku

Tokyo, Japan

Created Date

Sep 27, 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)

Endoscopic overtube, single-use - UK MHRA Medical Device Registration

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Last Updated

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Created Date

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DJ Fang

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