Cardiac radio-frequency ablation system catheter
- Device ID
- 98533
- MHRA Reference Number
- 98533
- Date Registered
- Nov 26, 2024
- Last Updated
- Jul 3, 2024
- Device Type
- General Medical Device
- Devices
- Cardiac radio-frequency ablation system catheter
- Type
- Class III
- Address
- 31 TECHNOLOGY DRIVE, SUITE 200 IRVINE, CALIFORNIA, United States
- Created Date
- Aug 25, 2021
- Relationship Type
- UK Responsible Person
- Address
- Baird House 4 Lower Gilmore Bank Edinburgh, Scotland, United KingdomPostcode: EH3 9QP
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by Johnson & Johnson Medical Ltd in the UK
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 98533. 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.