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$330.00
MakeBTNX Covid-19 Antibody Test Cassette
Model
Manufactuer ID20/PK

Coronavirus disease 2019 (COVID-19) is a respiratory illness that can spread from person to person. The virus is transmitted mainly via respiratory droplets that people sneeze, cough, or exhale. The incubation period for COVID-19 is currently estimated at between 2 and 14 days. The 2 main methods of diagnoses include Molecular Tests (RT-PCR) that identifies active infection in patients and Antibody Tests (IgG/IgM) which are specific to detecting antibodies indicating prior or current infection.

The Rapid Response Liberty COVID-19 IgG/IgM Test Cassette is a rapid, qualitative test for the detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-2 IgG antibodies in human whole blood, serum, or plasma samples.

PCR Validated Samples 98.4% Overall Positive Agreement 98.9% Overall Negative Agreement

Quick Results Interprets results in 10 minutes   

Interpretation of Test Results Negative - C line only Positive - C line and G line or M line

Easy to use :1. Add 10 μl of the venous whole blood, serum, or plasma.

                     2. Add 1 drop of the included buffer solution.

     


    $585.95
    Make BTNX Covid-19 Antigen tests
    Model
    Manufactuer ID20/PK

    The rapid COVID-19 Antigen Test is FDA Emergency Use Authorized, CLIA Waived, and allows for an efficient, accurate, and cost-friendly method of detection at the Point-of-Care. In just 10 minutes, the test is able to detect the SARS-CoV-2 nucleocapsid protein antigen through visual interpretation of colored lines.The SARS-CoV-2 nucleocapsid protein antigen is generally detectable in nasopharyngeal swab specimens during the acute phase of infection. This test is intended for individuals suspected of COVID-19 within five days of symptom onset.

    MANUFACTURED BY ACCESS BIO

    CLIA WAIVED CERTIFICATE ACCEPTABLE 

       


      $595.50
      MakeAcessBio
      ModelCarestart Covid-19 Antigen tests
      Manufactuer ID20/PK

      The CareStart™ COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from individuals who are suspected of COVID-19 by their healthcare providers. This product is CLIA waived under FDA/EUA authorization.

      Kit Component

      • 20 Test devices
      • 20 Assay buffer
      • 20 Extraction vials and caps
      • 20 Specimen collection swabs
      • 1 Positive and 1 negative
      • 1 Instructions for Use

      CLIA WAIVED CERTIFICATE ACCEPTABLE 

         

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