The BD Veritor™ Plus Analyzer provides reliable results in a timely manner, allowing you to quickly diagnose and treat your patients using an easy-to-read, portable device. Once you have bought the device, you can choose from a range of assays for a menu of respiratory tract infections.
The BD Veritor™ Plus System provides diagnostic testing where and when your patients need it, offering reliable, rapid results for a variety of respiratory tract infections.
Reliable results are important to help you confidently create treatment plans that fit your patients’ needs.
May reduce the potential for manual workflow errors by streamlining sample processing.
Because it can perform multiple tests, even in the same visit, the BD Veritor™ Plus Analyzer is cost-efficient.
The analyzer is small enough to be portable, so you can test where your patients are—and it provides workflow options for multitasking and efficiency.
The BD Veritor™ Plus System provides an easy sample-collection process that can be incorporated across a variety of clinical settings.
See how BD supports you with tools, education, and training—enabling a streamlined point-of-care experience for those you serve, and confidence in your results.
* The BD Veritor™ System for Rapid Detection of SARS-CoV-2 is intended for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in direct anterior nasal swabs from individuals who are either suspected of COVID-19 by their health care provider within the first five days of the onset of symptoms, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.
This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA for use by authorized laboratories.
RSV=respiratory syncytial virus; SARS-CoV-2=severe acute respiratory syndrome coronavirus 2.
This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens.
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.
Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C §263a, that meet the requirements to perform moderate, high or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.