Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping IVD, kit, agglutination - UK MHRA Medical Device Registration
Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping IVD, kit, agglutination is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 199143. The device is manufactured by Diapro Tıbbi Ürünler Sanayi ve Ticaret A.Ş. from Turkey, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Werfen 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
In Vitro Diagnostic Device
Devices
Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping IVD, kit, agglutination
Type
IVD Annex II List A
Date Registered
Nov 26, 2024
Last Updated
Aug 21, 2024
Address
İnönü Mah, Gebze Plastikçiler OSB Atatürk Blv. No:25/1 Gebze
Kocaeli, Turkey
Created Date
May 10, 2024
Name
Werfen LtdRelationship Type
Address
712 The Quadrant, Cavendish Avenue, Birchwood, Warrington WA3 6DE Manchester
Manchester, England, United Kingdom
Postcode: WA3 6DE
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