Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return - UK MHRA Medical Device Registration
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 107882. 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.
Device Type
General Medical Device
Devices
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Nov 5, 2024
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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