Histoplasma capsulatum antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Histoplasma capsulatum antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 128202. The device is manufactured by MiraVista Diagnostics LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U 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
Histoplasma capsulatum antigen IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Nov 19, 2024
Address
4705 Decatur Blvd.
Indianapolis, Indiana, United States
Created Date
Dec 24, 2021
Relationship Type
Address
7 CAMPION WAY
BINGHAM, NOTTINGHAM, England, United Kingdom
Postcode: NG13 8 TR
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