Rally #188-1-6088
BD #256088
BD Veritor™ Plus System SARS-CoV-2 & Flu A+B Kit (30 Test/KT)
Respiratory Test Kit, SARS-COV-2/FLU A+B, Rapid Chromatographic Digital Immunoassay, Anterior Nasal Swab, Rx Only
BD Veritor™ Mix & Match Promotional Offerings
Save On BD Veritor™ Rapid Antigen Tests!
Buy 4 BD Kits Of Any Combination, Get 1 at No Additional Cost
(1 Kit = 30 Tests)
Offer Valid Through March 31, 2025
Promotion Expired
See Details Below
Features
May help reduce manual test processing errors with its easy operation and single-button functionality
Displays easy-to-read digital results for COVID-19 and Flu A+B in 15 minutes
Provides clear, objective results by correcting for nonspecific binding and detecting positives not recognized by the unaided eye
Adapts easily to your workflow by offering 2 operational modes: Walk Away and Analyze Now
Captures or downloads the lot number, patient/specimen ID, operator ID, and test records using the BD Veritor™ InfoWiFi module
The BD Veritor™ System for Rapid Detection of SARS-CoV-2 & Flu A+B is a rapid chromatographic digital immunoassay intended for the in vitro, simultaneous qualitative detection and differentiation of SARS-CoV-2 nucleocapsid antigen and/or influenza A and B nucleoprotein antigens directly from anterior nasal swab samples taken from individuals who are suspected of a viral respiratory infection consistent with COVID-19 by a healthcare provider, within the first six days of symptom onset.
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.
This test is not intended to detect influenza C antigens. Results are for the simultaneous identification of SARS-CoV-2 nucleocapsid protein and Influenza A and B viral nucleoproteins.
Negative results should be treated as presumptive, do not rule out either Influenza or SARS-CoV-2, and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions.
Important Note:
Product is non-returnable; please make sure it is the right product before ordering.
If put into refrigeration, do not freeze.
For in vitro diagnostic use.
The test kit is intended for use with the analyzer.
For use under an Emergency Use Authorization (EUA) only.
For more information on this product's EUA, please go to the EUA section below.
For the State of California:
Warning: This product can expose you to chemicals known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov.
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Rally #
188-1-6088
Manufacturer #
256088
GTIN
00382902560883
Brand
BD Veritor™ System
Manufacturer
BD
Country of Origin
Unknown
Application
Respiratory Test Kit
For Use With
For use with the BD Veritor™ Plus Analyzer running Firmware version 5.50 or later
Murine and Leporine anti-SARS coronavirus, murine anti-flu A, anti-flu B and anti-biotin monoclonal antibodies conjugated to detector reagents are bound in the sample delivery area
Extraction Reagent
30 single use reaction tubes, each with 400 µL extraction reagent and having an integral dispensing tip
Detergent solution with less than 0.1% sodium azide (preservative)
Specimen Sampling Swabs
30 sterile, single use specimen sampling swabs
For sample collection and transfer
SARS-CoV-2 (+) Control Swab
1 each – individually wrapped for single use
SARS-CoV-2 antigen (inactive recombinant nucleocapsid protein) with less than 0.1% sodium azide
Flu A (+) Control Swab
1 each – individually wrapped for single use
Influenza A antigen (inactive recombinant nucleoprotein) with less than 0.1% sodium azide
Flu B (+) Control Swab
1 each – individually wrapped for single use
Influenza B antigen (inactive recombinant nucleoprotein) with less than 0.1% sodium azide
Paperboard Tube Stands
3 each
Each stand has capacity for 10 extraction reagent tubes
Assay Documentation
1 each – Instructions for use
1 each – Quick reference instruction card
1 each – Nasal sampling instructions
BD Veritor™ Plus System for Rapid Detection of Respiratory Syncytial Virus (RSV) CLIA-Waived
Note: Offer excludes Group A Strep kits and RSV Moderate Complexity kits.
To receive your promotional item(s), customers will need to complete a form provided by BD, and upload the proof of purchase.
The customer will receive a Proof of Purchase from Rally Inc. after purchasing the product. However, the promotional offer is handled solely between you, the customer, and the manufacturer, BD (Becton, Dickinson and Company). Rally Inc. does not oversee these offers. To check eligibility for the promotion and receive your promotional item, please follow the manufacturer's online instructions.
Note: Some items are under Emergency Use Authorization, please check their EUA before purchasing.
You can find more informations on this product's promotion and the required form
here.
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- Reimbursements Information -
This product maybe reimbursable, depending on various factors including current law and policies. Rally Inc. does not handle these reimbursements; instead, each reimbursement is handled solely between you, the customer, and the manufacturer, BD. Rally Inc. does not oversee these reimbursements. To check eligibility and get your reimbursements, please follow the manufacturer's reimbursements instructions.
You can find more informations on reimbursement details
here.
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EUA - Emergency Use Authorization
In the USA, this product has not been FDA cleared or approved; but has been authorized by FDA under an Emergency Use Authorization. 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 the virus that causes COVID-19 under Section 564(b)(1) of Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or the authorization is revoked sooner.
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