Cardiac mapping catheter, percutaneous, single-use - UK MHRA Medical Device Registration

Cardiac mapping catheter, percutaneous, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 98529. 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 mapping catheter, percutaneous, single-use

MHRA Device ID: 98529•Ref: 98529

Device Type

General Medical Device

Devices

Cardiac mapping catheter, percutaneous, single-use

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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Other Products from BIOSENSE WEBSTER, INC. (10)

Other Products from Same Authorized Representative (10)

Cardiac mapping catheter, percutaneous, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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