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EUROLINE Bordetella pertussis (IgG)

DN 2050-24001 G · EUROIMMUN Medizinische Labordiagnostika AG

Details

Device typeBordetella pertussis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA): A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin G (IgG) antibodies to Bordetella pertussis in a clinical specimen, using an enzyme immunoassay (EIA) method. The assay is designed to detect infection with Bordetella pertussis, the bacteria associated with whooping cough.

FDA categoryAntigen, B. Pertussis

Device ID04049016085478

Single useYes

MRI safetyLabeling does not contain MRI Safety Information

Contact

No contact is listed for this device.

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