Point-of-Care Testing
With Clarity and Confidence
Point-of-care testing with SARS-CoV-2,* Flu A+B, RSV, and Group A Strep assays, providing rapid diagnostic testing in a convenient, portable instrument.
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Built for care. Designed to adapt.
Why choose the rapid diagnostic testing of the BD Veritor Plus System?
Versatility
Diagnose multiple respiratory tract infections with the BD Veritor™ Plus System to help minimize their spread as well as reduce their duration.
Reliability
The advanced particle technology of the BD Veritor™ Plus System may improve test performance (when compared to visually read tests) by providing unambiguous professional-grade results.
Connectivity
Optional modules allow the BD Veritor™ Plus System to integrate seamlessly into your EMR/LIS and streamline your workflow to benefit your practice.
Discover how easy sample collection can simplify testing workflows for reliable results you can act on
The BD Veritor™ Plus System is a versatile and efficient rapid diagnostic testing program with robust support, giving you the ability to provide reliable results and decide on a course of treatment for your patients quickly at the point of care, and in the environment that makes them most comfortable.
In acute care settings—where health complexities, rapid decision-making, and workflow systems converge—it becomes easy to appreciate the effortlessness with which the BD Veritor™ Plus System accommodates changes in workflow and capacity.
Point-of-care rapid diagnostic testing has become increasingly essential, and the BD Veritor™ Plus System can make a big difference. In-house respiratory tract infection testing with reliable, rapid results means staff is more prepared for rapid triage; able to detect and diagnose infections and even treat a patient in the same visit.
As a community organization, you have many priorities, but we know you have people to protect. You require flexibility, simplicity and reliability, so that those you serve and those who work for you can continue to enjoy life. With the BD Veritor™ Plus System, you can identify certain respiratory infections and then take steps to limit the spread of these respiratory infections throughout your organization and the community.
Trust BD for the Digital Difference
Integrating workflows for reliable results you can act on.
Unambiguous, easy-to-read results displayed on a digital screen
A portable instrument, about the size of a smartphone
Maintenance-free and calibration-free instrumentation
Operational flexibility to meet your team’s workflow needs
Seamless results management and reporting via optional connectivity solutions
A rechargeable battery for up to 8 hours of continuous testing
Rapid results for multiple respiratory tract infections delivered in 15 minutes or less for increased efficiency
Single-button functionality to easily switch between operating modes
Simplified staff training and ongoing support with comprehensive training resources
Contact a Sales Representative to get your organization’s
diagnostic testing program started today
Useful Documents
Professional Care Testing
The BD Veritor™ Plus System enhances point-of-care testing for SARS-CoV-2,* Flu A+B, RSV, and Group A Strep assays, providing rapid diagnostic testing in a convenient, portable instrument.
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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.
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.
BD, the BD Logo, and BD Veritor are trademarks of Becton, Dickinson and Company or its affiliates. © 2025 BD. All rights reserved.
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