ERCP catheter, non-balloon, electrosurgical - UK MHRA Medical Device Registration

ERCP catheter, non-balloon, electrosurgical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95708. 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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ERCP catheter, non-balloon, electrosurgical

MHRA Device ID: 95708•Ref: 95708

Device Type

General Medical Device

Devices

ERCP catheter, non-balloon, electrosurgical

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jul 18, 2024

Manufacturer Information

Name

FUJIFILM Medwork GmbH

Address

Medworking 1

Höchstadt, Germany

Created Date

Aug 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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ERCP catheter, non-balloon, electrosurgical - UK MHRA Medical Device Registration

Device Type

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Date Registered

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