Chlamydia trachomatis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Chlamydia trachomatis immunoglobulin G (IgG) 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 208770. The device is manufactured by DIA.PRO Diagnostic Bioprobes S.r.l. from Italy, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Chlamydia trachomatis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 208770

Device Type

In Vitro Diagnostic Device

Type

IVD Annex II List B

Status

DREGIY

Date Registered

Jan 16, 2025

Manufacturer Information

Name

DIA.PRO Diagnostic Bioprobes S.r.l.

Address

Via Giosuè Carducci, 27, 20099 Sesto San, Giovanni

Milan, Italy

DJ Fang

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Chlamydia trachomatis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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Date Registered

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