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31% sensitivity and 99
quality management that conforms to ISO 9001 and ISO 13485
Do not expose the test devices and extraction solutions to temperatures outside of room temperature during testing
Tests/box 25 Detects Multiple HCV genotypes Sample type Fingerstick and Venipuncture whole blood collection Time to results 20 minutes Accuracy Greater than 98%
increasing confidence in results External controls included Facilitates internal laboratory quality control Room temperature storage No refrigerator space needed
GenBody COVID-19 Ag Test coming soon 31% sensitivity and 99For In Vitro Diagnostic Use. For Prescription Use Only. For Professional Use Only. For Emergency Use Authorization (EUA) Only. The GenBody COVID 19 Ag is an immunochromatographic rapid diagnostic test (RDT) intended for the qualitative detection of nucleocapsid protein antigen from SARS CoV 2 in direct nasopharyngeal (NP) or anterior nasal (AN) swab specimens from individuals who are suspected of COVID 19 by their healthcare provider within the first
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