United Kingdom MHRA device registration 126256

Cancer associated serum antigen (CASA) IVD, kit, enzyme immunoassay (EIA)

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Rhythm Biosciences Limited·Registered Dec 22, 2021
Registration details
Device ID
126256
MHRA Reference Number
126256
Date Registered
Dec 22, 2021
Last Updated
Nov 12, 2022
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Cancer associated serum antigen (CASA) IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Manufacturer
Address
Bio 21 Molecular Science & Biotechnology Building 30 Flemington Road
Parkville, Victoria, Australia
Created Date
Dec 22, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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About this record

Cancer associated serum antigen (CASA) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 126256. The device is manufactured by Rhythm Biosciences Limited from Australia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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