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

Chlamydia trachomatis 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 211986. The device is manufactured by Virion\Serion GmbH from Germany, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Chlamydia trachomatis immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 211986

Device Type

In Vitro Diagnostic Device

Type

Class C

Status

DREGIY

Date Registered

Feb 27, 2025

Manufacturer Information

Name

Virion\Serion GmbH

Address

Friedrich-Bergius-Ring 19

Wurzburg, Germany

DJ Fang

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

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Date Registered

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