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 145958. The device is manufactured by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Boston Scientific Limited.
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Device Type
General Medical Device
Devices
Endocardial defibrillation lead
Type
Class III
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
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