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

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 107883. The device is manufactured by Andocor NV from Belgium, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, Ltd. .

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, drainage

MHRA Device ID: 107883•Ref: 107883

Device Type

General Medical Device

Devices

Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 5, 2024

Manufacturer Information

Name

Andocor NV

Address

Kwikaard 104

Zoersel, Belgium

Created Date

Oct 12, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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