Cardiopulmonary bypass system centrifugal pump - UK MHRA Medical Device Registration
Cardiopulmonary bypass system centrifugal pump is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 84939. The device is manufactured by Maquet Cardiopulmonary GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Getinge 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.
Device Type
General Medical Device
Devices
Cardiopulmonary bypass system centrifugal pump
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Jul 24, 2024
Name
Getinge LimitedRelationship Type
Address
Unit 3 St Modwen Park Andressey Way Chaddesden
Derby, England, United Kingdom
Postcode: DE21 6YH
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