Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Calibrators / Calibrator Kit / Calibrator Kit Vitros® SARS-CoV-2 Antigen 2 X 1 mL For use with Vitros SARS-CoV-2 Antigen Test / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems Liquid6199950
Picture of Calibrator Kit Vitros® SARS-CoV-2 Antigen 2 X 1 mL For use with Vitros SARS-CoV-2 Antigen Test / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems Liquid6199950

Calibrator Kit Vitros® SARS-CoV-2 Antigen 2 X 1 mL For use with Vitros SARS-CoV-2 Antigen Test / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems Liquid6199950

Calibrator-Kit-Vitros®-SARS-CoV-2-Antigen-2-X-1-mL-For-use-with-Vitros-SARS-CoV-2-Antigen-Test--For-use-on-the-VITROS-3600-Immunodiagnostic-System-and-the-VITROS-5600--XT-7600-Integrated-Systems-Liquid6199950

SKU #

#1180546

MPN #

6199950

Brand

Ortho Clinical Diagnostics

Stock

In Stock

Quantity

100

Features

CALIBRATOR, VITROS SARS-COV-2 ANTIGEN 1 LEVEL 2X1ML D/S

$85.82 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1180546
Manufacturer # 6199950
Brand Vitros®
Manufacturer Ortho Clinical Diagnostics
Application Calibrator Kit
Container Type Vial
For Use With For use with Vitros SARS-CoV-2 Antigen Test / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems
Form Liquid
Levels 1 Level
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Storage Requirements Keep Frozen
Test Name SARS-CoV-2 Antigen
UNSPSC Code 41116128
Volume 2 X 1 mL
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  • The Vitros SARS-CoV-2 Antigen Reagent Pack used in combination with the Vitros SARS-CoV-2 Antigen Calibrator is for use under an FDA EUA only: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
  • Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C 263a, that meet the requirements to perform moderate or high complexity tests
  • EUA will be effective until the declaration that circumstances exist justifying the authorization of the emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 is terminated under Section 564(b)(2) of the Act or the EUA is revoked under Section 564(g) of the Act
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health laboratories
  • Negative results from patients with symptom onset outside of one to six days should be treated as presumptive
  • 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, 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
  • 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
  • Includes: 2 vials of VITROS SARS-CoV-2 Antigen Calibrator (recombinant SARS-CoV-2 nucleocapsid antigen in buffer with bovine serum albumin and antimicrobial agent, 1.0 mL) and 8 calibrator bar code labels