Premier Biotech COVID-19 IgG/ IgM Antibody Test Cassette CLIA Waived

Premier Biotech

Premier Biotech COVID-19 IgG/ IgM Antibody Test Cassette CLIA Waived

Premier Biotech
SKU: 550798
MFG Part #: RT-CV19-20
  • RightSign™ COVID-19 IgG/IgM Rapid Test Cassette is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection
  • RightSign™ COVID-19 IgG/IgM Rapid Test Cassette should not be used to diagnose acute SARS-CoV-2 infection
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
  • False positive results may occur due to cross-reactivity from pre-existing antibodies or other possible causes
  • Due to the risk of false positive results, confirmation of positive results should be considered using second, different IgG or IgM assay
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    Price:
    $226.73 20 / Box

    Description

    Premier Biotech RT-CV19-20 COVID-19 IgG/ IgM Rapid Test Cassette (CLIA WAIVED) (Whole Blood/ Serum/ Plasma).

    Features

    • Testing of serum, plasma and venous whole blood specimens is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, that meet requirements to perform moderate or high complexity testsAND NO LONGER AVAILABLE
    • Testing of fingerstick whole blood specimens 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 high, moderate or waived complexity tests
    • Testing of fingerstick whole blood specimens 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
    • RightSign™ COVID-19 IgG/IgM Rapid Test Cassette is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection
    • RightSign™ COVID-19 IgG/IgM Rapid Test Cassette should not be used to diagnose acute SARS-CoV-2 infection
    • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
    • False positive results may occur due to cross-reactivity from pre-existing antibodies or other possible causes
    • Due to the risk of false positive results, confirmation of positive results should be considered using second, different IgG or IgM assay
    • RightSign™ COVID-19 IgG/IgM Rapid Test Cassette is a rapid lateral flow chromatographic immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in in human venous whole blood (sodium heparin, EDTA, and sodium citrate), serum or plasma (sodium heparin, potassium EDTA and sodium citrate)
    • This test uses anti-human IgM antibody (test line IgM), anti-human IgG (test line IgG) and goat anti-mouse IgG (control line C) immobilized on a nitrocellulose strip
    • This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb3(b)(1), unless the authorization is terminated or revoked sooner

    Product Specifications and Resources

    Number of Tests 20 Tests
    Reading Type Visual Read
    Sample Type Whole Blood / Serum / Plasma Sample
    Technology Lateral Flow Technology
    Test Format Cassette Format
    Test Method Rapid Chromatographic Immunoassay
    Test Name COVID-19 IgG / IgM
    Test Type Antibody Test
    Time to Results 10 Minute Results
    Volume 3 mL Buffer
    UNSPSC Code 41116205
    What's in the Box
  • (20) Cassettes
  • 1 X 3 mL Buffer
  • (20) Capillaries
  • Package Insert
  • Procedure Card
  • (20) Lancets
  • (20) Pads

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