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 172848. The device is manufactured by Terumo Cardiovascular Systems Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Terumo UK Ltd.
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Device Type
General Medical Device
Devices
Cardiopulmonary bypass system centrifugal pump
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 2, 2024
Address
125 Blue Ball Road
Elkton, Maryland, United States
Created Date
Apr 29, 2021
Name
Terumo UK LtdRelationship Type
Address
Otium House 2 Freemantle Road
Bagshot, Surrey, England, United Kingdom
Postcode: GU19 5LL
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