Kit Rapid Test BD Veritor™ System Infectious Disease Immunoassay SARS-CoV-2 Nasal Swab Sample 30 Tests by BD ID 256082

188-1-6082
      
Stock Est. Shipping Date: 29th April 2025

Kit Rapid Test BD Veritor™ System Infectious Disease Immunoassay SARS-CoV-2 Nasal Swab Sample 30 Tests
Sold by: KT OF 30

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Rally #188-1-6082
BD #256082
BD Veritor™ Plus System SARS-CoV-2 Kit (30 Test/KT)

Respiratory Test Kit, SARS-COV-2, 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


See Details Below
Features
  • Helps reduce manual test processing errors with its easy operation and single-button functionality
  • Provides intuitive sample processing with prefilled, unitized tubes
  • Displays easy-to-read digital results for COVID-19 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
  • 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
The BD Veritor™ System for Rapid Detection of SARS-CoV-2 is a chromatographic digital immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal swab specimens collected by a healthcare provider from individuals suspected of COVID-19 within the first 5 days of symptom onset when tested at least twice over 3 days with at least 48 hours between tests and from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested at least three times over 5 days with at least 48 hours between 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.

The BD Veritor™ System for Rapid Detection of SARS-CoV-2 does not differentiate between SARS-CoV and SARS-CoV-2. Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen, which is generally detectable in anterior nasal swab specimens during the acute phase of infection.

All negative results are presumptive and confirmation with a molecular assay, if necessary for patient management, may be performed. Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management 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.
  • Test kits 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 #188-1-6082
Manufacturer #256082
GTIN00382902560821
BrandBD Veritor™ System
ManufacturerBD
Country of OriginUnknown
ApplicationRespiratory Test Kit
For Use WithFor use with the BD Veritor™ Plus Analyzer running Firmware version 5.4 or later
Number of Tests30 Tests
Reading TypeMachine Read
Sample TypeAnterior Nasal Swab Sample
SpecialtyImmunoassay
Test FormatTest Device Format
Test Kit TypeRapid
Test MethodChromatographic Digital Immunoassay
Test NameSARS-CoV-2
Time to Results15 Minute Results
UNSPSC Code41116144
Storage Temperature2-30 °C (Do not Freeze)
Shelf Life (Days)300

Type PPA NPA Results In
COVID-19 (SARS-CoV-2) 84%
(95% CI, 67%-93%)
100%
(95% CI, 98%-100%)
15 minutes

PPA = positive percent agreement
NPA = negative percent agreement



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Configurations
Product ID Description Unit of Measure
256066 BD Veritor™ Plus Analyzer 1/EA
256082 BD Veritor™ Plus System SARS-CoV-2 Kit 30 Tests/Kit
256084 Combo Veritor Plus SARS-COV-2 KIT (2 Kits of 256082 + 1 of 256066 Analyzer) 1 Kit
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BD Veritor™ for SARS-CoV-2 Kit - 256082 Contents:
Kit Component Quantity Description
BD Veritor™ System Test Devices 30 single use test devices Foil pouched test device containing one reactive strip. Each strip has one line of murine anti-SARS coronavirus monoclonal antibody on the test line, and one of biotin coupled to bovine protein on the positive control line. Murine and Leporine anti-SARS coronavirus 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 325 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 Non-infectious, recombinant viral protein antigen with less than 0.1% sodium azide.
SARS-CoV-2 (–) Control Swab 1 each – individually wrapped for single use Buffer with less than 0.1% sodium azide.
Assay Documentation 1 each – Instructions for use
1 each – Quick reference instruction card
1 each – Nasal sampling instructions

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BD Veritor™ Mix & Match Promotional Offer

Save on BD Veritor™ rapid antigen tests!

Buy 4 kits, get 1 at no additional cost.
(1 Kit = 30 Tests)

Mix & Match: Promotional offerings available in any combination (below).

Offer valid through March 31, 2025 Only.

Promotional Items
BD Item NumberDescription
256088 BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 & Influenza A+B
256082 BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2
256045 BD Veritor™ Plus System for Rapid Detection of Influenza A+B CLIA-Waived
256041 BD Veritor™ Plus System for Rapid Detection of Influenza A+B (moderate complexity)
256038 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 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.

This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. 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.


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