Ordering & Reimbursement

Prepare your order in four simple steps:

Select product options to create a customized PDF you can print and send to your distributor representative

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Select the BD Veritor™ Plus Analyzer

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Select assays

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Add options

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Contact distributor or sales to place your order

Not sure which distributor to order from? We’re here to help.

Compatible printers for reporting options

There are several receipt and label printer models compatible with the BD Veritor™ Plus System, ready for use out of box, including:

Epson® TM-T20II: Receipt printer uses 3-inch (80mm) wide roll paper and includes and auto cutter.

Epson® TM-m30: Receipt printer uses 3-inch (80mm) wide roll paper and includes and auto cutter. Sold in a starter kit through NETS-PG with customer print cable and paper included.

Epson® TM-T20: Functionality equivalent to the TM-T20II. Offered in some worldwide regions instead of the T20II.

These printers are not sold through BD or BD Veritor™ Plus System distributors (e.g. McKesson, Medline, Concordance, etc.) but are sold through Epson® printer distributors such as NETS-PG (orders through www.nets-pg.com/BD-orders, or phone 603-552-5513) and other vendors (e.g. Amazon, Staples, etc.).

BD Veritor™ Plus System training

Simplify staff training with our e-Learning platform. Includes assay training modules, how-to videos, dashboards and more.

Quick start guide

Everything you need to know to set up your BD Veritor™ Plus System

Reimbursement FAQs

**The BD Veritor™ Plus System for Rapid Detection of SARS-CoV-2 & Flu A+B is intended for the qualitative detection of SARS-CoV-2 and/or influenza A and B nucleocapsid 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 product has not been FDA cleared or approved; but has been authorized by FDA under an EUA for use by authorized laboratories.

•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.

•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.