United Kingdom MHRA device registration 208783
Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay
United Kingdom·In Vitro Diagnostic Device·DIA.PRO Diagnostic Bioprobes S.r.l.·Registered Jan 16, 2025DREGIYRegistration details
- Device ID
- 208783
- Status
- DREGIY
- Date Registered
- Jan 16, 2025
Device classification
- Device Type
- In Vitro Diagnostic Device
- Type
- IVD Annex II List B
Manufacturer
- Address
- Via Giosuè Carducci, 27, 20099 Sesto San, Giovanni Milan, Italy
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About this record
Toxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 208783. The device is manufactured by DIA.PRO Diagnostic Bioprobes S.r.l. from Italy, classified as In Vitro Diagnostic Device.
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