Endocardial defibrillation lead - UK MHRA Medical Device Registration

Endocardial defibrillation lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 200130. The device is manufactured by Abbott Medical from United States, classified as General Medical Device. The authorized representative in the UK is Abbott Medical UK Limited.

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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Endocardial defibrillation lead

MHRA Device ID: 200130•Ref: 200130

Device Type

General Medical Device

Devices

Endocardial defibrillation lead

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 4, 2024

Manufacturer Information

Name

Abbott Medical

Address

15900 Valley View Court

Sylmar, California, United States

Created Date

Sep 21, 2022

Authorized Representative

Name

Abbott Medical UK Limited

Relationship Type

UK Responsible Person

Address

Elder House Central Boulevard Blythe Valley Business Park

Solihull, West Midlands, England, United Kingdom

Postcode: B90 8AJ

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Endocardial defibrillation lead - UK MHRA Medical Device Registration

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