Bartonella bacilliformis immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration
Bartonella bacilliformis immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120850. The device is manufactured by DiaSorin Molecular LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is DiaSorin Italia S.p.A. UK Branch.
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
Bartonella bacilliformis immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Jun 7, 2024
Address
11331 Valley View St.
Cypress, California, United States
Created Date
Nov 23, 2021
Relationship Type
Address
Central Road
Dartford, England, United Kingdom
Postcode: DA1 5LR
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