Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Toxoplasma gondii 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 208779. The device is manufactured by DIA.PRO Diagnostic Bioprobes S.r.l. from Italy, classified as In Vitro Diagnostic Device.
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Device Type
In Vitro Diagnostic Device
Type
IVD Annex II List B
Status
Date Registered
Jan 16, 2025
Address
Via Giosuรจ Carducci, 27, 20099 Sesto San, Giovanni
Milan, Italy
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