Cardioplegia solution administration kit - UK MHRA Medical Device Registration
Cardioplegia solution administration kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 73431. The device is manufactured by Terumo Europe NV from Belgium, classified as General Medical Device. The authorized representative in the UK is Terumo 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
Cardioplegia solution administration kit
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 2, 2024
Name
Terumo UK LtdRelationship Type
Address
Otium House 2 Freemantle Road
Bagshot, Surrey, England, United Kingdom
Postcode: GU19 5LL
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