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that meet the requirements to perform moderate
This is the initial laboratory test used for people with signs or symptoms
observed collection to detect recent drug use with results in minutes
preventative maintenance* FDA-cleared and CLIA-waived* For Point-of-Care molecular PCR testing* Results available in under 30 minutes* Enables single-visit “test and treat”* Integrates with EMR/LISContents: 1 io Instrument1 Main Power Cable with Plug1 External Power Supply1 io Instrument Operator Manual1 io Instrument Repackaging Instruction Sheet
Status COVID-19/Flu A&B Rapid Antigen Test (33225) dip stick that meet the requirements toStatus COVID 19 Flu A&B test is a lateral flow immunoassay intended for the in vitro rapid, simultaneous qualitative detection and differentiation of nucleocapsid antigen from SARS CoV 2, influenza A and or influenza B directly from nasopharyngeal swab specimens obtained from individuals, who are suspected of respiratory viral infection consistent with COVID 19 by their healthcare provider, within the first five days of onset of symptoms. Product