Endoscopic procedure air/water valve, single-use - UK MHRA Medical Device Registration

Endoscopic procedure air/water valve, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 102269. The device is manufactured by FUJIFILM Medwork GmbH from Germany, 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 procedure air/water valve, single-use

MHRA Device ID: 102269•Ref: 102269

Device Type

General Medical Device

Devices

Endoscopic procedure air/water valve, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 18, 2024

Manufacturer Information

Name

FUJIFILM Medwork GmbH

Address

1 Medworkring

Höchstadt, Germany

Created Date

Sep 2, 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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Endoscopic procedure air/water valve, single-use - UK MHRA Medical Device Registration

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