Flexible endoscopic biopsy forceps, single-use - UK MHRA Medical Device Registration

Flexible endoscopic biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95699. 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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Flexible endoscopic biopsy forceps, single-use

MHRA Device ID: 95699•Ref: 95699

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class IIa

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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Flexible endoscopic biopsy forceps, single-use - UK MHRA Medical Device Registration

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Name

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Created Date

Name

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