Pacing/defibrillation lead tunneller - UK MHRA Medical Device Registration

Pacing/defibrillation lead tunneller is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 71662. The device is manufactured by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Boston Scientific 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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MHRA Registered

Active implantable device (Directive 90/385/EEC only)

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Pacing/defibrillation lead tunneller

MHRA Device ID: 71662

Device Type

Active implantable device (Directive 90/385/EEC only)

Devices

Pacing/defibrillation lead tunneller

Type

Active implantable Medical device

Date Registered

Apr 1, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation

Address

4100 Hamline Avenue North

St. Paul, Minnesota, United States

Created Date

Apr 1, 2021

Authorized Representative

Name

Boston Scientific Limited

Relationship Type

UK Responsible Person

Address

100 New Bridge Street

London, England, United Kingdom

Postcode: EC4V 6JA

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Pacing/defibrillation lead tunneller - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

Pacing/defibrillation lead tunneller

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