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

Toxoplasma gondii 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 74253. 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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Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 74253•Ref: 74253

Device Type

In Vitro Diagnostic Device

Devices

Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD Annex II List B

Date Registered

Oct 27, 2024

Last Updated

Apr 5, 2024

Manufacturer Information

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

DJ Fang

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

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