Complement component C3a IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Complement component C3a IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138132. The device is manufactured by Quidel Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.
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
Complement component C3a IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 10, 2023
Address
2005 East State Street, Suite 100
Athens, OH, United States
Created Date
Feb 25, 2022
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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