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AMERICAN BIOMEDICA CORPORATION

American Bio Medica Corporation is a biotechnology company that develops, manufactures and markets accurate, cost-effective immunoassay test kits, including point-of-collection tests for drugs of abuse.
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Covid-19 AMERICAN BIOMEDICA CORPORATION

Clinical Laboratory

COVID-19 IgG/IgM Test
COVID-19 IgG/IgM Rapid Test

The COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood / Serum / Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to 2019 Novel Coronavirus in human whole blood, serum or plasma.
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COVID-19 Detection Kit
Logix Smart COVID-19 Detection Kit (US FDA EUA/CE-IVD)

The Logix Smart COVID-19 Detection Kit (US FDA EUA/CE-IVD) is an in vitro diagnostic test that uses the company’s patented CoPrimer technology for the qualitative detection of the RNA from SARS-CoV-2 coronavirus (COVID-19). The test operates using a single step real-time reverse transcriptase polymerase chain reaction (RT-PCR) process in lower respiratory tract fluids (e.g. bronchoalveolar lavage, sputum, tracheal aspirate), and upper respiratory tract fluids (e.g. nasopharyngeal and oropharyngeal swabs) from suspected COVID-19 patients.
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COVID-19 Antigen Test (Swab)
Rapid COVID-19 Antigen Test (Swab)

The Rapid COVID-19 Antigen Test (Swab) is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) swab specimens directly from individuals who are suspected of Covid-19 by their healthcare provider.
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About AMERICAN BIOMEDICA CORPORATION

American Bio Medica Corporation is a biotechnology company that develops, manufactures and markets accurate, cost-effective immunoassay test kits, including point-of-collection tests for drugs of abuse.
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COVID-19 Antigen Test (Swab)

COVID-19 Antigen Test (Swab)

Model: Rapid COVID-19 Antigen Test (Swab)
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Description:

The Rapid COVID-19 Antigen Test (Swab) is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) swab specimens directly from individuals who are suspected of Covid-19 by their healthcare provider.

Features

Features

Clinical Evaluation
• Positive Percent Agreement (PPA): 95.7%
• Negative Percent Agreement (NPA): 99.6%
• Overall Percent Agreement (OPA): 98.9%
20 tests per box Request Information

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