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Description
The LifeSign Status COVID-19 Flu Influenza A & B Rapid Antigen Test is a rapid immunoassay that can be used to simultaneously detect and diagnose SARS-CoV-2, Influenza Type A, and Type B antigens. The test is quick and easy to use, with results visible in just 15 minutes. It is also highly accurate, with a sensitivity of 97.7% and a specificity of 100%. This makes it an essential tool for anyone who wants to check for the presence of these viruses. The flocked nasopharyngeal swab included with the kit ensures superior specimen collection and patient comfort. The test is Health Canada approved and has also been approved for use under FDA Emergency Use Authorization (EUA).
Features
- 1 test + 1 specimen = 3 Results
- Visually read in 15 minutes.
- Flocked nasopharyngeal swab for superior specimen collection and patient comfort.
- Results are for the simultaneous identification of nucleocapsid antigens of SARS-CoV-2, influenza A and influenza B, but do not differentiate between SARS-CoV and SARS-CoV-2 viruses and are not intended to detect influenza C antigens.
- Approved under FDA Emergency Use Authorization (EUA).
- Health Canada approved.
Product Specifications
| Sample Type: | Nasopharyngeal Swab Sample |
|---|---|
| Test Type: | Antigen Detection |
| Time to Results: | 15 Minutes Results |
| CLIA complexity: | Waived, Moderate, or High |
| Number of Tests: | 25 Tests |
| Reading Type: | Visual Read |
| Test Format: | Test Device Format |
| Test Method: | Lateral Flow Immunoassay |
|---|---|
| Test Type: | Antigen Detection |
| Time to Results: | 15 Minute Results |
| COVID 19: | Sensitivity 93.9%, Specificity 100%. |
| Flu A: | Sensitivity 91.4%, Specificity 95.7%. |
| Flu B: | Sensitivity 87.6%, Specificity 95.9%. |
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Frequently Asked Questions (FAQs)
Covid - CPT Code: 87811QW, Flu A CPT Code: 87804QW, Flu B CPT Code: 87804QW-59
The Lifesign Status COVID-19 / Flu Influenza A & B Rapid Antigen Test provides results in approximately 15 minutes after the sample is applied to the test device. It offers a relatively quick turnaround time compared to some other diagnostic tests, aiding prompt decision-making and management of potential COVID-19 and flu cases.
The Lifesign Status COVID-19 / Flu Influenza A & B Rapid Antigen Test may have obtained authorization or approval from regulatory agencies, such as the U.S. Food and Drug Administration (FDA).
They are Proudly made in the USA