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Respiratory Test Kit Sofia® 2 Sars Antigen+ 25 Tests Clia Waived

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Respiratory Test Kit Sofia® 2 Sars Antigen+ 25 Tests Clia Waived

  • Sofia 2 SARS Antigen+ FIA received De Novo FDA clearance on March 8, 2023
  • Sofia 2 SARS Antigen+ Fluorescent Immunoassay (FIA), uses advanced immunofluorescence-based lateral flow technology in a sandwich design for qualitative detection of nucleocapsid protein from SARS-CoV-2
  • The Sofia 2 SARS Antigen+ FIA, with the Sofia 2 analyzer, provides automated and objective results in 10 minutes, allowing for COVID-19 testing of symptomatic patients when serial testing is started within 6 days of symptom onset
  • Sofia 2 SARS Antigen+ FIA is the first FDA-cleared, 10-minute rapid antigen test for COVID-19
  • Rapid results to support efficient dispositioning of patients
  • Reliable results without cross-reactivity to seasonal coronaviruses
  • Virena connection: Provides automated tracking, data capture, government reporting, and exclusive disease mapping
  • Ready for use with Sofia 2 for nasal swab procedure
  • Includes positive and negative controls
  • The test does not differentiate between SARS-CoV and SARS-CoV-2
  • A negative test result is presumptive, and it is recommended these results be confirmed by a molecular SARS-CoV-2 assay
  • Negative results do not preclude SARS-CoV-2 infections and should not be used as the sole basis for treatment or other patient management decisions
  • Positive results do not rule out co-infection with other respiratory pathogens
  • This test is intended for prescription use only and can be used in Point-of-Care settings
  • Materials Not Supplied in Kit: Timer or watch, Sofia 2 Instrument, Calibration Cassette
  • Sofia 2 SARS Antigen+ FIA received De Novo FDA clearance on March 8, 2023
  • Sofia 2 SARS Antigen+ Fluorescent Immunoassay (FIA), uses advanced immunofluorescence-based lateral flow technology in a sandwich design for qualitative detection of nucleocapsid protein from SARS-CoV-2
  • The Sofia 2 SARS Antigen+ FIA, with the Sofia 2 analyzer, provides automated and objective results in 10 minutes, allowing for COVID-19 testing of symptomatic patients when serial testing is started within 6 days of symptom onset
  • Sofia 2 SARS Antigen+ FIA is the first FDA-cleared, 10-minute rapid antigen test for COVID-19
  • Rapid results to support efficient dispositioning of patients
  • Reliable results without cross-reactivity to seasonal coronaviruses
  • Virena connection: Provides automated tracking, data capture, government reporting, and exclusive disease mapping
  • Ready for use with Sofia 2 for nasal swab procedure
  • Includes positive and negative controls
  • The test does not differentiate between SARS-CoV and SARS-CoV-2
  • A negative test result is presumptive, and it is recommended these results be confirmed by a molecular SARS-CoV-2 assay
  • Negative results do not preclude SARS-CoV-2 infections and should not be used as the sole basis for treatment or other patient management decisions
  • Positive results do not rule out co-infection with other respiratory pathogens
  • This test is intended for prescription use only and can be used in Point-of-Care settings
  • Materials Not Supplied in Kit: Timer or watch, Sofia 2 Instrument, Calibration Cassette
Select Packaging
From $166.03

Original: $553.45

-70%
Respiratory Test Kit Sofia® 2 Sars Antigen+ 25 Tests Clia Waived

$553.45

$166.03

Description

  • Sofia 2 SARS Antigen+ FIA received De Novo FDA clearance on March 8, 2023
  • Sofia 2 SARS Antigen+ Fluorescent Immunoassay (FIA), uses advanced immunofluorescence-based lateral flow technology in a sandwich design for qualitative detection of nucleocapsid protein from SARS-CoV-2
  • The Sofia 2 SARS Antigen+ FIA, with the Sofia 2 analyzer, provides automated and objective results in 10 minutes, allowing for COVID-19 testing of symptomatic patients when serial testing is started within 6 days of symptom onset
  • Sofia 2 SARS Antigen+ FIA is the first FDA-cleared, 10-minute rapid antigen test for COVID-19
  • Rapid results to support efficient dispositioning of patients
  • Reliable results without cross-reactivity to seasonal coronaviruses
  • Virena connection: Provides automated tracking, data capture, government reporting, and exclusive disease mapping
  • Ready for use with Sofia 2 for nasal swab procedure
  • Includes positive and negative controls
  • The test does not differentiate between SARS-CoV and SARS-CoV-2
  • A negative test result is presumptive, and it is recommended these results be confirmed by a molecular SARS-CoV-2 assay
  • Negative results do not preclude SARS-CoV-2 infections and should not be used as the sole basis for treatment or other patient management decisions
  • Positive results do not rule out co-infection with other respiratory pathogens
  • This test is intended for prescription use only and can be used in Point-of-Care settings
  • Materials Not Supplied in Kit: Timer or watch, Sofia 2 Instrument, Calibration Cassette