United Kingdom MHRA device registration 74266

Treponema pallidum immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·Dia.Pro Diagnostic Bioprobes S.r.l.·Registered Oct 25, 2024

Registration details

Device ID: 74266
MHRA Reference Number: 74266
Date Registered: Oct 25, 2024
Last Updated: Apr 5, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Treponema pallidum immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: Dia.Pro Diagnostic Bioprobes S.r.l.
Address: 27 Via Giosue Carducci SESTO SAN GIOVANNI
MI, Lombardia, Italy
Created Date: Apr 20, 2021

Authorized Representative

Name: Launch Diagnostics Limited
Relationship Type: UK Responsible Person
Address: Unit 20 Ash Way Thorp Arch Estate
Wetherby, England, United Kingdom
Postcode: LS23 7FA

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About this record

Treponema pallidum immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 74266. The device is manufactured by Dia.Pro Diagnostic Bioprobes S.r.l. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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