Home / Clinical Laboratory / Test Kits / Rapid Test Kit / Rapid Test Kit BD Veritor™ System Infectious Disease Immunoassay SARS-CoV-2 Nasal Swab Sample 30 Tests256082
Picture of Rapid Test Kit BD Veritor™ System Infectious Disease Immunoassay SARS-CoV-2 Nasal Swab Sample 30 Tests256082

Rapid Test Kit BD Veritor™ System Infectious Disease Immunoassay SARS-CoV-2 Nasal Swab Sample 30 Tests256082

Rapid-Test-Kit-BD-Veritor™-System-Infectious-Disease-Immunoassay-SARS-CoV-2-Nasal-Swab-Sample-30-Tests256082

SKU #

#1170197

MPN #

256082

Brand

BD Primary Care

Stock

In Stock

Quantity

100

Features

TEST KIT, SARS-COV-2 BD VERITOR RAPID DETECT (30TEST/KT)

$643.67 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1170197
Manufacturer # 256082
Brand BD Veritor™ System
Manufacturer BD Primary Care
Application Rapid Test Kit
Contents (30) Single-use Test Devices, (30) Single-use Reaction Tubes, (30) Sterile Single-use Specimen Sampling Swabs, Positive SARS-CoV-2 Control Swab, Negative SARS-CoV-2 Control Swab, Instructions for Use, Quick Reference Card, Nasal Sampling Instructions
For Use With For use with the BD Veritor™ Plus Analyzer running Firmware version 5.4 or later
Number of Tests 30 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 30 days
Reading Type Machine Read
Sample Type Nasal Swab Sample
Storage Requirements USP Controlled Room Temperature
Test Format Test Device
Test Method Chromatographic Digital
Test Name SARS-CoV-2
Test Type Infectious Disease Immunoassay
Time To Results 15 Minute Results
UNSPSC Code 41116144
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  • Product ships from McKesson with minimum 30 days dating
  • The BD Veritor™ System for Rapid Detection of SARS-CoV-2 is for use under an Emergency Use Authorization ONLY: https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2
  • 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
  • Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status
  • Positive results do not rule out bacterial infection or co-infection with other viruses
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
  • Negative results should be treated as presumptive, do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions
  • Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management
  • The BD Veritor System for Rapid Detection of SARS-CoV-2 is intended for use by trained clinical laboratory personnel specifically instructed and trained in the techniques of in vitro diagnostic procedures, and proper infection control procedures and individuals similarly trained in point of care settings
  • In the United States, the BD Veritor™ System for Rapid Detection of SARS-CoV-2 is only for use under the Food and Drug Administration’s Emergency Use Authorization