SARS-CoV-2 neutralizing antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration
SARS-CoV-2 neutralizing antibody IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68881. The device is manufactured by Diasia Biomedical Technology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CMC Medical Devices 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
SARS-CoV-2 neutralizing antibody IVD, kit, rapid ICT, clinical
Type
IVD General
Date Registered
Mar 8, 2021
Last Updated
Nov 9, 2022
Address
3th B, 4th Floor, Building No.4, Chuangfu Industrial Park, Xixiang Tiegang Reservoir Road, Baoan District,
Shenzhen, China
Created Date
Mar 8, 2021
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
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