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 205962. The device is manufactured by Vitatron Holding B.V. from Netherlands, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
General Medical Device
Type
Class III
Status
Date Registered
Dec 21, 2024
Address
Endepolsdomein 5
Maastricht, Netherlands
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Registered: Mar 26, 2021
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Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 26, 2021
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