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 71664. The device is manufactured by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Boston Scientific 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.
Device Type
Active implantable device (Directive 90/385/EEC only)
Devices
Endocardial defibrillation lead
Type
Active implantable Medical device
Date Registered
Apr 1, 2021
Last Updated
Dec 22, 2022
Address
4100 Hamline Avenue North
St. Paul, Minnesota, United States
Created Date
Apr 1, 2021
Relationship Type
Address
100 New Bridge Street
London, England, United Kingdom
Postcode: EC4V 6JA
Endocardial defibrillation lead
Type: General Medical Device
Manufacturer: BIOTRONIK SE & Co. KG
Endocardial defibrillation lead
Type: Active Implantable Device
Manufacturer: Medtronic, Inc
Endocardial defibrillation lead
Type: General Medical Device
Manufacturer: Microport CRM S.r.l
Endocardial defibrillation lead
Type: Active Implantable Device
Manufacturer: St. Jude Medical Cardiac Rhythm Management Division
Endocardial defibrillation lead
Type: General Medical Device
Manufacturer: Medtronic, Inc
Endocardial defibrillation lead
Type: Active Implantable Device
Manufacturer: BIOTRONIK SE & Co. KG
Endocardial defibrillation lead
Type: General Medical Device
Manufacturer: Abbott Medical
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