BD Veritor™ System
for SARS-CoV-2

The BD Veritor™ System test for COVID-19 that is reliable and simple-to-operate.

 

Now 510k Cleared

 

Contact Us

 

Hero - 510k Cleared COVID test

Simplifying COVID-19 testing.

When your patients need reliable, rapid COVID-19 testing, turn to the BD Veritor™ System.

 

It offers dependable results at the point of care in a simple-to-operate portable instrument.

White and orange packing box with blue lettering for BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 & Flu A+B test

Clinical performance vs RT-PCR

 

PPA

NPA

Results in

COVID-19

(SARS-CoV-2)

84%

(95% C.I. 77.2%-89.1%)

99.7%

(95% C.I. 99.0%-99.9%)

 

15 minutes

 

 

COVID-19 results in 15 minutes

positive percent agreement

negative percent agreement

 

Ordering information

Cat no.

Qty

BD Veritor™ System SARS-CoV-2 

256092

30 tests

BD Veritor™ Plus Analyzer

256066

1 unit

Get more answers with every sample.

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Simplifies the testing process

  • Helps reduce manual test processing errors with its easy operation and single-button functionality
  • Provides intuitive sample processing with prefilled, unitized tubes
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Delivers workflow efficiency

Adapts easily to your workflow by offering 2 operational modes

  • Walk Away: the test device is inserted immediately into the Analyzer so staff can multitask while the sample incubates (15 minutes)
  • Analyze Now: the test device is inserted after the incubation time is complete, allowing batches of samples to be tested (results in seconds)
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Provides results traceability

  • Stores or downloads the lot number, patient/ specimen ID, operator ID and test records using the BD Veritor™ InfoWiFi module or via the companion ImageMover application
  • Offers result printing capabilities via USB port
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Achieves reliable, rapid results

Displays easy-to-read digital results for COVID-19 in 15 minutes:

  • “CoV2: +” for positive; “CoV2: –” for negative

Provides clear, objective results by correcting for nonspecific binding and detecting faint lines not recognized by the unaided eye3

Contact a Sales Representative to get your organization’s

diagnostic testing program started today

How It Works

The BD Veritor™ Plus System provides an easy sample-collection process that can be incorporated across a variety of clinical settings.

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Step 1: Collect sample

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Step 2: Mix the swab with the reagent vial

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Step 3: Prepare assay with the sample

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Step 4: Run the test

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Step 5: Insert the cartridge and read the results

BD Veritor™ Plus System Support & Training

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.

Professional Care Testing

The BD Veritor™ Plus System enhances point-of-care testing for COVID-19, Flu A+B, COVID-19 & Flu A+B,* RSV and Group A Strep, providing rapid diagnostic testing in a convenient, portable instrument.

1. BD Veritor™ System for SARS-CoV-2. Package insert. 500075511(01) Becton, Dickinson and Company.

BD Life Sciences, 7 Loveton Circle, Sparks, MD 21152-0999 USA 800-638-8663

 

*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.