SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration
SARS-CoV-2 immunoglobulin G (IgG)/IgM 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 197065. The device is manufactured by Zhejiang Orient Gene Biotech Co. Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SENSUS Group 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 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Jul 25, 2024
Address
3787#, East Yangguang Avenue, Dipu Street Anji, Huzhou
Zhejiang, China
Created Date
Aug 20, 2021
Name
SENSUS Group LtdRelationship Type
Address
The Barn Tednambury Farm Tednambury
Spellbrook, Hertfordshire, England, United Kingdom
Postcode: CM23 4BD
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