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 85492. The device is manufactured by Cook Incorporated from United States, 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: 85492•Ref: 85492

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 Incorporated

Address

750 Daniels Way

Bloomington, Indiana, United States

Created Date

Feb 23, 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

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

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Address

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