Percutaneous radio-frequency ablation system generator - UK MHRA Medical Device Registration

Percutaneous radio-frequency ablation system generator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 64952. 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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Percutaneous radio-frequency ablation system generator

MHRA Device ID: 64952•Ref: 64952

Device Type

General Medical Device

Devices

Percutaneous radio-frequency ablation system generator

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

BIOSENSE WEBSTER, INC

Address

33 TECHNOLOGY DRIVE

IRVINE , CALIFORNIA, United States

Created Date

Jan 27, 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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Percutaneous radio-frequency ablation system generator - 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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Address

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