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Trinity Biotech

B. Pertussis PT/FHA EIA Test System, EIA for the detection of antibody to Bordetella pertussis PT and FHA, 96 Tests

Details

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

FDA categoryAntigen, B. Pertussis

Device ID05391516747899

Catalog number40-6196P

Single useYes

MRI safetyLabeling does not contain MRI Safety Information

Contact

Phone800-325-3424

Emailinfo@trinitybiotech.com

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