Home / Clinical Laboratory / Clinical Laboratory Accessories / Antigen Extraction Buffer / Antigen Extraction Buffer Vitros® 28 mL For use to Extract the Viral Load from Swab Samples Placed in Appropriate Transport Media / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems6199944
Picture of Antigen Extraction Buffer Vitros® 28 mL For use to Extract the Viral Load from Swab Samples Placed in Appropriate Transport Media / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems6199944

Antigen Extraction Buffer Vitros® 28 mL For use to Extract the Viral Load from Swab Samples Placed in Appropriate Transport Media / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems6199944

Antigen-Extraction-Buffer-Vitros®-28-mL-For-use-to-Extract-the-Viral-Load-from-Swab-Samples-Placed-in-Appropriate-Transport-Media--For-use-on-the-VITROS-3600-Immunodiagnostic-System-and-the-VITROS-5600--XT-7600-Integrated-Systems6199944

SKU #

#1180548

MPN #

6199944

Brand

Ortho Clinical Diagnostics

Stock

In Stock

Quantity

100

Features

BUFFER, ANTIGEN EXTRACTION SARS-COV-2 (1000T/EA) D/S

$311.11 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1180548
Manufacturer # 6199944
Brand Vitros®
Manufacturer Ortho Clinical Diagnostics
Application Antigen Extraction Buffer
For Use With For use to Extract the Viral Load from Swab Samples Placed in Appropriate Transport Media / For use on the VITROS 3600 Immunodiagnostic System and the VITROS 5600 / XT 7600 Integrated Systems
Specifications 28 mL
UNSPSC Code 41116128
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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
  • The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen test is a chemiluminescent immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasopharyngeal (NP) specimens from individuals who are suspected of COVID-19 by their healthcare provider within one to six days of the onset of symptoms using the VITROS 3600 Immunodiagnostic System and the VITROS 5600/XT 7600 Integrated Systems
  • 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 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
  • 1 extraction buffer pack containing: 4 bottles of VITROS SARS-CoV-2 Antigen Extraction Buffer (28 mL) with antimicrobial agent
  • Rx only; For in vitro diagnostic and laboratory professional use