BD Veritor™ Plus System
for Rapid Detection of
Flu A+B

The BD Veritor™ Plus System test for Flu A and Flu B that is simple, efficient, and fast.

 

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BD Veritor All Assays

Overcome the challenges of flu season.

The BD Veritor™ Plus System offers simple operation, an efficient workflow, and fast, traceable results, which may help improve the patient experience.

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

BD Veritor™ Plus System for Rapid Detection of Flu A+B (CLIA-waived kit) offers proven performance vs PCR

 

PPA

NPA

Results in

Influenza A

CLIA-waived

83.6%

(76.1%, 89.1%)

97.5%

(95.7%, 98.5%)

 

10 minutes

 

Influenza B

CLIA-waived

81.3%

 (71.1%, 88.5%)

98.2%

(95.7%, 99.3%)

10 minutes

 

Flu A+B results in 10 minutes

†positive percent agreement

‡negative percent agreement

 

Ordering information

Cat no.

Qty

BD Veritor™ Plus System Flu A+B CLIA-waived kit

256045

30 tests

BD Veritor™ Plus System Flu A+B moderately complex kit

256041

30 tests

Get more answers with every sample.

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Simplifies the testing process

  • Helps user operation with single-button functionality that can potentially reduce manual test processing errors
  • 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 into the Analyzer immediately after preparation, allowing staff to multitask while the sample incubates
  • Analyze Now: the test device is inserted after the incubation time is complete, allowing batches of samples to be tested at once
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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 flu in just 10 minutes1
  • Provides clear, objective results by correcting for nonspecific binding and detecting faint lines not recognized by the unaided eye4

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™ Plus System for Rapid Detection of Flu A+B. Package insert. 8087667 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.