Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Reagents / Reagent with Calibrator Kit / Reagent with Calibrator Kit Advia Centaur® Antibody Test SARS-CoV-2 IgG For use with ADVIA Centaur XP and ADVIA Centaur XPT Systems 500 Tests 3 X 10 mL11206993
Picture of Reagent with Calibrator Kit Advia Centaur® Antibody Test SARS-CoV-2 IgG For use with ADVIA Centaur XP and ADVIA Centaur XPT Systems 500 Tests 3 X 10 mL11206993

Reagent with Calibrator Kit Advia Centaur® Antibody Test SARS-CoV-2 IgG For use with ADVIA Centaur XP and ADVIA Centaur XPT Systems 500 Tests 3 X 10 mL11206993

Reagent-with-Calibrator-Kit-Advia-Centaur®-Antibody-Test-SARS-CoV-2-IgG-For-use-with-ADVIA-Centaur-XP-and-ADVIA-Centaur-XPT-Systems-500-Tests-3-X-10-mL11206993

SKU #

#1173390

MPN #

11206993

Brand

Siemens

Stock

In Stock

Quantity

100

Features

REAGENT, CENTAUR COV2G 2X1ML LOW 2X1ML HIGH (500TST/KT) D/S

$3,617.11 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1173390
Manufacturer # 11206993
Brand ADVIA Centaur®
Manufacturer Siemens
Application Reagent with Calibrator Kit
Container Type Vial
For Use With For use with ADVIA Centaur XP and ADVIA Centaur XPT Systems
Number of Tests 500 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Sample Type Human Serum / Plasma Sample
Storage Requirements Requires Refrigeration
Test Name SARS-CoV-2 IgG
Test Type Antibody Test
Type Chemiluminescent Immunoassay
UNSPSC Code 41116020
Volume 3 X 10 mL
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  • SARS-CoV-2 IgG (COV2G) is ONLY for use under FDA Emergency Use Authorization: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
  • Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C 263a, that meet requirements to perform moderate or high complexity tests
  • The ADVIA Centaur SARS-CoV-2 IgG (COV2G) assay is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection
  • At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity
  • The ADVIA Centaur SARS-CoV-2 IgG (COV2G) assay should not be used to diagnose acute SARS-CoV-2 infection
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
  • The sensitivity of the ADVIA Centaur SARS-CoV-2 IgG (COV2G) assay early after infection is unknown; negative results do not preclude acute SARS-CoV-2 infection
  • If acute infection is suspected, direct testing for SARS-CoV-2 is necessary
  • False positive results for the ADVIA Centaur SARS-CoV-2 IgG (COV2G) assay may occur due to cross-reactivity from pre-existing antibodies or other possible causes
  • Includes (5) ReadyPack® primary reagents, 2 X 1 mL vial high calibrator and 2 X 1 mL vial low calibrator