Once you have bought the BD Veritor™ Plus Analyzer, you can then order various compatible assays to deliver reliable respiratory infection testing.
The BD Veritor™ Plus System is a point-of-care testing solution for SARS-CoV-2, SARS-CoV-2 & Flu A+B,* Flu A+B, Group A Strep, and RSV. It offers:
Unambiguous positive/negative display which may help to reduce result interpretation errors and streamline diagnosis.
Delivers digitally read results in 15 minutes or less,** supporting timely clinical decisions.
No monthly calibration required, operated with single-button functionality.
No service contracts, maintenance or calibration needed for device lifetime.
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.
Order the BD Veritor™ Plus Analyzer and system accessories. Browse our CPT codes for various rapid antigen assays, including Flu and COVID-19.
RSV=respiratory syncytial virus; SARS-CoV-2=severe acute respiratory syndrome coronavirus 2.
*In the USA, the BD Veritor™ System for Rapid Detection of SARS-CoV-2 & Flu A+B has not been FDA cleared or approved but has been authorized by the FDA under an Emergency Use Authorization for use by authorized laboratories; use by laboratories certified under the CLIA, 42 U.S.C. §263a, that meet requirements to perform moderate, high, or waived complexity tests. The product 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.
This product has been authorized only for the detection of proteins from SARS-CoV-2, influenza A and influenza B, not for any other viruses or pathogens; and, in the USA, the emergency use of 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.
**Result processing times for each BD Veritor™ assay are 15 minutes for the SARS-CoV-2 and SARS-CoV-2 & Flu A+B assays, 10 minutes for Flu A+B and RSV assays, and 5 minutes for the Group A Strep assay.
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