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 82209. The device is manufactured by Cook Ireland Ltd from Ireland, classified as General Medical Device. The authorized representative in the UK is Cook (UK) Ltd.

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: 82209•Ref: 82209

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 8, 2024

Manufacturer Information

Name

Cook Ireland Ltd

Address

O'Halloran Road National Technology Park

Limerick, Ireland

Created Date

Mar 2, 2021

Authorized Representative

Name

Cook (UK) Ltd

Relationship Type

UK Responsible Person

Address

3rd Floor, 1 Ashley Road

Altrincham, Cheshire, England, United Kingdom

Postcode: WA14 2DT

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

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