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BD Veritor™ Plus System Documents

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BD Veritor™ Plus System Overview Brochure


BD Veritor™ for SARS-CoV-2 & Flu A+B

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BD Veritor™ SARS-CoV-2 and Flu A+B Sell Sheet

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BD Veritor™ SARS-CoV-2 & Flu A + B Emergency Use Authorization (EUA) letter

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BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 & Flu A+B Instructions for Use

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BD Veritor™ Plus System SARS-CoV-2 & Flu A+B Assay Fact Sheet for Healthcare Providers

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BD Veritor™ Plus System SARS-CoV-2 & Flu A+B Assay Fact Sheet for Patients


BD Veritor™ for SARS-CoV-2

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BD Veritor™ SARS-CoV-2 Sell Sheet

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BD Veritor™ SARS-CoV-2 Emergency Use Authorization (EUA) letter

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BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 Instructions for Use

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BD Veritor™ Plus System SARS-CoV-2 Assay Fact Sheet for Healthcare Providers

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BD Veritor™ Plus System SARS-CoV-2 Assay Fact Sheet for Patients

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Quick Reference Instructions for BD Veritor™ Plus System SARS-CoV-2


BD Veritor™ for Flu A+B

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BD Veritor™ Flu A+B Sell Sheet

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BD Veritor™ Plus Sytem for Rapid Detection of Flu A+B Instructions for Use

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BD Veritor™ Plus Sytem for Rapid Detection of Flu A+B Quick Reference Guide

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BD Veritor™ Plus Sytem for Rapid Detection of Flu A+B CLIA-Waived Instructions for Use

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BD Veritor™ Plus System for Rapid Detection of Flu A+B CLIA-Waived Quick Reference Guide

BD Veritor™ for Flu A+B products meet the FDA Class II special controls applicable to RIDTs for analytical reactivity testing.
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Annual flu strain reactivity testing results - BD Veritor Flu A+B CLIA waived kit 2023

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Annual flu strain reactivity testing results - BD Veritor Flu A+B laboratory kit 2023

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Annual flu strain reactivity testing results - BD Veritor Flu A+B CLIA waived kit 2021

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Annual flu strain reactivity testing results - BD Veritor Flu A+B laboratory kit 2021

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Annual flu strain reactivity testing results - BD Veritor Flu A+B CLIA waived kit 2020

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Annual flu strain reactivity testing results - BD Veritor Flu A+B laboratory kit 2020

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What you need to know about RIDTs


BD Veritor™ for RSV

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BD Veritor™ RSV Sell Sheet

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BD Veritor™ Plus System for Rapid Detection of RSV Instructions for Use

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BD Veritor™ Plus System for Rapid Detection of RSV Quick Reference Guide

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BD Veritor™ Plus System for Rapid Detection of RSV CLIA-Waived Instructions for Use

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BD Veritor™ Plus System for Rapid Detection of RSV CLIA-Waived Quick Reference Guide


BD Veritor™ for Group A Strep

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BD Veritor™ for Group A Strep Sell Sheet

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BD Veritor™ Plus System for Rapid Detection of Group A Strep Instructions for Use

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BD Veritor™ Plus Sytem for Rapid Detection of Group A Strep Quick Reference Guide


Contact our Sales Team

To request a demo or for more information about our products, contact our Sales Representatives.

The BD Veritor™ Plus System

Be more prepared to take care of the people you serve with the rapid diagnostic testing of the versatile BD Veritor™ Plus System. 

Buying Options

Order the BD Veritor™ Plus Analyzer, assays and accessories.

* 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.