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 156947. The device is manufactured by BIOTRONIK SE & Co. KG from Germany, classified as General Medical Device. The authorized representative in the UK is BIOTRONIK UK 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.

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Endocardial defibrillation lead

MHRA Device ID: 156947•Ref: 156947

Device Type

General Medical Device

Devices

Endocardial defibrillation lead

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Mar 6, 2024

Manufacturer Information

Name

BIOTRONIK SE & Co. KG

Address

Woermannkehre 1

Berlin, Germany

Created Date

Mar 8, 2021

Authorized Representative

Name

BIOTRONIK UK LIMITED

Relationship Type

UK Responsible Person

Address

BIOTRONIK House, Avonbury Business Park

Bicester, United Kingdom

Postcode: OX26 2UA

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Endocardial defibrillation lead - UK MHRA Medical Device Registration

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