Hepatitis E virus immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration
Hepatitis E virus immunoglobulin M (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 173500. The device is manufactured by Hangzhou Alltest Biotech Co Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap 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
Hepatitis E virus immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Jun 15, 2024
Address
#550 Yinhai Street Hangzhou Economic & Technological Development Area
Hangzhou, China
Created Date
Mar 9, 2021
Name
Medimap LtdRelationship Type
Address
2 The Drift
Thurston, Suffolk, United Kingdom
Postcode: IP31 3RT
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