The BD Veritor At-Home COVID-19 Test lets you know if you’re “positive” or “negative” in as fast as 15 minutes. This test is the first to use smartphones to read, interpret, and display results so you can read your results in words, not lines. The BD Veritor At-Home COVID-19 Test uses the same hospital-grade technology that clinicians trust, ensuring accurate results at the tip of your fingers. This test is reimbursable and FSA and HSA eligible.
Zero guesswork with the Scanwell Health app: Unlike other rapid tests that involve manual interpretation of lines, the BD Veritor At-Home COVID-19 test uses computer vision technology to interpret the results for you. After collecting your sample with the nasal swab and mixing it with the reagent, wait for 15 minutes then scan it with the Scanwell Health app. The app will interpret and translate the results into the words “negative” or “positive”. This eliminates guesswork and reduces the risk for user interpretation errors. If your result is positive, the app will automatically report it to your state agencies. You can also save, share, and print your results using the app.
Easy and pain-free nasal swab: Collecting your swab is done in 5 easy steps with included written and video (in-app) instructions. The kit includes everything you need to complete the test. This is an over-the-counter test with no lab or prescription needed.
Advanced detection technology: This COVID-19 at-home test is an antigen test that detects the nucleocapsid protein antigen produced by the SARS-CoV-2 virus. One kit includes two sets of tests to encourage serial testing or the practice of taking the tests within 48 hours of each other. It can be used for adults and children as young as 2 years old.
With the BD Veritor At-Home COVID-19 Test, you can keep yourself, your family, and the larger community safe by staying home and getting tested.
FDA Disclaimers:
- This test is not FDA cleared or approved.
- It has been authorized by the FDA under an Emergency Use Authorization for use by authorized laboratories.
- It has been authorized only for detecting proteins from SARS-CoV-2 and not for any other viruses or pathogens.
- This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for the detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1) unless the authorization is terminated or revoked sooner.
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