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Respiratory Test Kit, Rapid Flu A/B & COVID-19 At Home Multiplex Rapid Test, Contents Include: (1) Test Cassette, (1) Swab, (1) Tube with Sample Processing Solution, (1) Quick Ref Instructions, SOLD as 10/Box by Tyfast, CorDx ACT21002110

Only for Medical Professional

Item#: Cor-ACT21002110-BX
$88.98
Item(s) Total: $88.98
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  • Product Details
    • Dealer # 1257160
    Manufacturer #s ACT21002110
    Brand Tyfast
    Manufacturer CorDx Inc
    Country of Origin United States
    Application Respiratory Test Kit
    Contents 1 (1) Test Cassette, (1) Swab, (1) Tube with Sample Processing Solution, (1) Quick Ref Instructions
    Number of Tests 1 Test per Kit
    Reading Type Visual Read
    Sample Type Anterior Nasal Swab Sample
    Specialty Immunoassay
    Test Format Cassette Format
    Test Kit Type Rapid
    Test Method Immunochromatographic Membrane Assay
    Test Name Flu A/B & COVID-19 At Home Multiplex Rapid Test
    Time to Results 10 Minute Results
    UNSPSC Code 41116144

    Features

    • CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test is for use under an FDA Emergency Use Authorization (EUA) only: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2
    • The CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test is a lateral flow immunoassay intended for the qualitative detection and differentiation of SARS-CoV-2, influenza A, and influenza B protein antigens
    • This test is authorized for non-prescription home use with self-collected anterior nasal swab specimens from individuals aged 14 years or older, or with adult-collected anterior nasal swab specimens from individuals two (2) years or older
    • This test is only authorized for individuals with signs and symptoms of respiratory infection consistent with COVID-19 within the first five (5) days of symptom onset when tested at least twice over three days with at least 48 hours between tests
    • Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status
    • Positive results do not rule out bacterial infection or co-infection with other viruses
    • All negative results are presumptive and confirmation with a molecular assay, if necessary for patient management, may be performed
    • Negative results do not rule out SARS-CoV-2, influenza A, and influenza B infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions such as isolating from others and wearing masks
    • Easy to use design, effortless self-administration, whether at home or on the go
    • Swift Clarity: Receive results rapidly in 10 minutes for early decision-making
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