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#1001192773 | Mfg #256087 | Clinical Laboratory

Control Swab Set BD Veritor™ SARS-CoV-2 Positive Level / Negative Level

SWAB SET, CONTROL SARS-COV-2 BD VERITOR SYSTEM (10/KT)
Control Swab Set BD Veritor™ SARS-CoV-2 Positive Level / Negative Level

BD Veritor System for Rapid Detection of SARS-CoV-2 and Flu A+B 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

Product Specifications

MSFH #
1001192773
Manufacturer #
256087
Brand
BD Veritor™
Manufacturer
BD
Country of Origin
Unknown
Application
Control Swab Set
For Use With
For use with the BD Veritor™ System for Rapid Detection of SARS-CoV-2 Assay as External Quality Control Materials
Levels
Positive Level / Negative Level
Test Name
SARS-CoV-2
UNSPSC Code
41116145

Description

This product is only for use under Emergency Use Authorization in 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 and operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation

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

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 SARS-CoV-2 results to the appropriate public health authorities

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

Negative results shoul d be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with one of these infections

Negative results for SARS-CoV-2 should be confirmed with a molecular assay, if necessary, for patient management

The BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B is intended for use in point of care settings by trained healthcare professionals or other users specifically instructed in the use of BD Veritor Systems and proper infection control procedures

Includes: 10 SARS CoV-2 Negative Control Swabs, 10 SARS CoV-2 Positive Control Swabs, and Instructions for use

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