Endocardial/interventricular septal pacing lead - UK MHRA Medical Device Registration
Endocardial/interventricular septal pacing lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183485. The device is manufactured by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class III
Status
Date Registered
Dec 21, 2024
Address
4100 Hamline Avenue North
St. Paul, Minnesota, United States
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