BD Veritor Plus COVID-19 Rapid Test Analyzer


Covid Tests


Learn About The BD Veritor Plus Analyzer

The BD Veritor Plus System has been designed as a reliable, rapid diagnostic testing system that delivers results at the point of care, so you can be more prepared to take care of the people you serve.

The BD Veritor Plus Analyzer is a portable, easy-to-use instrument that allows you to overcome challenges to providing streamlined POC testing. The BD Veritor Plus System is the rapid antigen testing solution designed to work with you and your team. The system offers fast and reliable results, with two analysis modes to seamlessly integrate into your workflow.

  • Offers flexible and adaptable workflow options, allowing you to maximize staff efficiency
  • Minimizes manual transcription by allowing data storage/download via USB port
  • Delivers timely results — 15 minutes for SARS-CoV-2,1 less than 11 minutes for Flu A+B2 and RSV,3 and less than 6 minutes for Group A Strep4 — minimizing patient wait times
  • Includes the interactive BD eLearning online training platform, providing a comprehensive curriculum

BD Veritor Plus Analyzer Overview:

The BD Veritor Plus System simplifies operation by offering:

  • Easy-to-use tests, allowing novice and non-lab personnel to confidently help with diagnosis of SARS-CoV-2, Flu A+B, RSV, and Group A Strep
  • Intuitive, single-button functionality, reducing training time
  • A digital display for easy-to-read results

    The intended use of the BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 assay only includes those who are suspected of COVID-19 by their health care provider within the first five days of the onset of symptoms. This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA for use by authorized laboratories. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens and this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

    Information for CLIA Certificate of Waivers:

    • BD Veritor™ Plus System tests can only be used in labs that are CLIA certified. A ‘lab’ refers to a facility that performs diagnostic tests from samples collected from the body. Naturally, that includes hospitals and clinical laboratories but also can include pharmacies, schools, long-term care facilities, and some businesses. These non-traditional locations can use the BD Veritor™ System tests and other simple CLIA-waived tests if they apply and are granted a CLIA certificate of Waiver. These non-traditional facilities can apply for a CLIA Certificate of Waiver at
    • Some diagnostic testing may be CLIA-waived, and include BD VeritorTM Plus System rapid antigen testing for SARS-CoV-2*, Flu A+B, Group A Strep and RSV.

    Complete information, additional resources, and how to videos can be found on the BD website.

    BD Veritor Plus Analyzer Specs:

    • Easy-to-read display featuring single-button functionality and minimal hands-on time to meet your staff’s demands
    • Flexible workflow options to adapt to your workplace needs
    • Timely, reliable results (15 minutes for SARS-CoV-21 ; <11 minutes for Flu A+B2 and RSV3 ; <6 minutes for Group A Strep4 ), minimizing wait times
    • BD eLearning online training platform that simplifies staff instruction and system implementation
    • Improved quality control and traceability enabled by the optional BD Veritor™ InfoScan module


    Resources to Aid Setting Up Covid-19 Diagnostic Testing Program:

    Additional Information:

    The BD Veritor Plus COVID-19 Rapid Test Analyzer is a quick and easy way to test for the presence of the COVID-19 virus. Simply insert the test strip into the analyzer and get results in as little as 15 minutes. This analyzer is 99.6% accurate and is FDA-cleared for emergency use.