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 187142. The device is manufactured by Biorad Medisys Pvt Ltd from India, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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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Endomyocardial biopsy forceps, single-use

MHRA Device ID: 187142•Ref: 187142

Device Type

General Medical Device

Devices

Endomyocardial biopsy forceps, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 23, 2024

Manufacturer Information

Name

Biorad Medisys Pvt Ltd

Address

Survey No.: 48/3 &48/7, Pashan Sus Road, Sus Village, Taluka Mulshi, Pune - 411021, Maharashtra, INDIA

Pune, Maharashtra, India

Created Date

Nov 3, 2021

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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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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Created Date

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