Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous - UK MHRA Medical Device Registration

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 93280. The device is manufactured by Medtronic, Inc from United States, classified as General Medical Device. 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.

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Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

MHRA Device ID: 93280•Ref: 93280

Device Type

General Medical Device

Devices

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 16, 2023

Manufacturer Information

Name

Medtronic, Inc

Address

710 Medtronic Parkway

Minneapolis, MN, United States

Created Date

Feb 2, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

Name

Relationship Type

Address

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