Cardiac radio-frequency ablation system catheter - UK MHRA Medical Device Registration

Cardiac radio-frequency ablation system catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 140231. The device is manufactured by BIOSENSE WEBSTER, INC. from United States, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical 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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Cardiac radio-frequency ablation system catheter

MHRA Device ID: 140231•Ref: 140231

Device Type

General Medical Device

Devices

Cardiac radio-frequency ablation system catheter

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 3, 2024

Manufacturer Information

Name

BIOSENSE WEBSTER, INC.

Address

31 TECHNOLOGY DRIVE, SUITE 200

IRVINE, CALIFORNIA, United States

Created Date

Aug 25, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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Cardiac radio-frequency ablation system catheter - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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