Rubella virus immunoglobulin M (IgM) antibody IVD, control - UK MHRA Medical Device Registration
Rubella virus immunoglobulin M (IgM) antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99665. The device is manufactured by LGC Clinical Diagnostics, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is QCS International 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
Rubella virus immunoglobulin M (IgM) antibody IVD, control
Type
IVD Annex II List B
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Address
37 Birch Street
Milford, Massachusetts, United States
Created Date
Apr 30, 2021
Relationship Type
Address
Suite 9 Cumbernauld Business Park Wardpark Road
Cumbernauld, North Lanarkshire, Scotland, United Kingdom
Postcode: G67 3JZ
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