Endocardial pacing lead - UK MHRA Medical Device Registration
Endocardial pacing lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 72001. The device is manufactured by Vitatron Holding B.V. from Netherlands, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Medtronic 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 pacing lead
Type
Active implantable Medical device
Date Registered
Mar 26, 2021
Last Updated
Dec 22, 2022
Relationship Type
Address
Building 9 Croxley Park
Watford, Herts, England, United Kingdom
Postcode: WD18 8WW
Endocardial pacing lead
Type: Active Implantable Device
Manufacturer: Medtronic, Inc
Endocardial pacing lead
Type: Active Implantable Device
Manufacturer: Microport CRM S.r.l
Endocardial pacing lead
Type: General Medical Device
Manufacturer: Microport CRM S.r.l
Endocardial pacing lead
Type: General Medical Device
Manufacturer: Microport CRM S.r.l
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Stimwave Technologies Incorporated
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Type: General Medical Device
Registered: Dec 21, 2024
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Type: Active implantable device (Directive 90/385/EEC only)
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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Type: General Medical Device
Registered: Mar 26, 2021
Dual-chamber implantable pacemaker, demand
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 26, 2021
Endocardial pacing lead
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 26, 2021
Single-chamber implantable pacemaker, fixed-rate/demand
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 26, 2021
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Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 26, 2021
Cardiac pulse generator software
Type: Active implantable device (Directive 90/385/EEC only)
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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Type: General Medical Device
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Type: General Medical Device
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Suction system canister liner
Type: General Medical Device
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Argon-enhanced electrosurgical system gas delivery unit
Type: General Medical Device
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Frame/rail/pole device holder
Type: General Medical Device
Manufacturer: SonarMed Inc

