United Kingdom MHRA device registration 207620
Toxoplasma gondii immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA)
United Kingdom·In Vitro Diagnostic Device·bioMérieux S.A·Registered Dec 21, 2024DREGIYRegistration details
- Device ID
- 207620
- Status
- DREGIY
- Date Registered
- Dec 21, 2024
Device classification
- Device Type
- In Vitro Diagnostic Device
- Type
- Class C
Manufacturer
- Name
- bioMérieux S.A
- Address
- bioMérieux S.AMarcy L'Etoile (69280), France
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About this record
Toxoplasma gondii immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207620. The device is manufactured by bioMérieux S.A from France, classified as In Vitro Diagnostic Device.
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