LifeSign Status™ COVID-19 Flu A&B
Status™ COVID-19/Flu test is a lateral flow immunoassay intended for the in vitro rapid, simultaneous qualitative detection and differentiation of nucleocapsid antigen from SARS-CoV2, influenza A and 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. Clinical signs and symptoms of respiratory viral infection due to SARS-CoV-2 and influenza can be similar. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet the requirements to perform moderate, high, or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

Test type: Lateral flow immunoassay
Specimen type: Nasopharyngeal (NP) swab specimen
Turnaround time: 15-20 minutes
FDA status: EUA granted
CLIA complexity: Waived, Moderate, or High
Specimen type: Nasopharyngeal (NP) swab specimen
Turnaround time: 15-20 minutes
FDA status: EUA granted
CLIA complexity: Waived, Moderate, or High
Ordering information:
Contact your Cardinal Health Laboratory Products Representative to order or complete the form below.
Material # | Description | Pkg string | Shipping UOM |
---|---|---|---|
33225 | Rapid SARS-CoV-2/Flu A&B Antigen combination test kit (25 EA/BX) | 25 EA/BX, 15 BX/CS | CS |
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Related information
Product insert
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718KB – PDF
Fact sheet for patients
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200KB – PDF
Fact sheet for healthcare providers
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231KB – PDF
During this extraordinary time, Cardinal Health strives to provide customers with accurate product information but relies on the manufacturer for updates. Please visit the manufacturer's product website for the most current information.