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

Multiple Chlamydia species 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 88466. The device is manufactured by Virion\Serion GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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In Vitro Diagnostic Device

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

MHRA Device ID: 88466•Ref: 88466

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD Annex II List B

Date Registered

Jul 12, 2021

Last Updated

Oct 13, 2022

Manufacturer Information

Name

Virion\Serion GmbH

Address

Friedrich-Bergius-Ring 19

Wurzburg, Germany

Created Date

Jul 12, 2021

Authorized Representative

Name

Launch Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Ash House Ash Road New Ash Green

Longfield, Kent, United Kingdom

Postcode: DA3 8JD

DJ Fang

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

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