Endomyocardial biopsy forceps, single-use - UK MHRA Medical Device Registration

Endomyocardial biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 156613. The device is manufactured by Cordis US Corp. from United States, classified as General Medical Device. The authorized representative in the UK is Cordis Medical 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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Endomyocardial biopsy forceps, single-use

MHRA Device ID: 156613•Ref: 156613

Device Type

General Medical Device

Devices

Endomyocardial biopsy forceps, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Nov 10, 2023

Manufacturer Information

Name

Cordis US Corp.

Address

14201 North West 60th Avenue

Miami Lakes, Florida, United States

Created Date

Sep 23, 2022

Authorized Representative

Name

Cordis Medical UK Limited

Relationship Type

UK Responsible Person

Address

Suite 402, Chadwick House Birchwood Park

Warrington, England, United Kingdom

Postcode: WA3 6AE

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Endomyocardial 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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