Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Reagents / Reagent with Calibrator Kit / Reagent with Calibrator Kit Atellica® IM Antibody Test SARS-CoV-2 IgG For use with Atellica® IM Analyzer 500 Tests 3 X 10 mL11206998
Picture of Reagent with Calibrator Kit Atellica® IM Antibody Test SARS-CoV-2 IgG For use with Atellica® IM Analyzer 500 Tests 3 X 10 mL11206998

Reagent with Calibrator Kit Atellica® IM Antibody Test SARS-CoV-2 IgG For use with Atellica® IM Analyzer 500 Tests 3 X 10 mL11206998

Reagent-with-Calibrator-Kit-Atellica®-IM-Antibody-Test-SARS-CoV-2-IgG-For-use-with-Atellica®-IM-Analyzer-500-Tests-3-X-10-mL11206998

SKU #

#1173393

MPN #

11206998

Brand

Siemens

Stock

In Stock

Quantity

100

Features

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

$3,617.11 USD

Attribute Name Attribute Value
McKesson # 1173393
Manufacturer # 11206998
Brand Atellica® IM
Manufacturer Siemens
Application Reagent with Calibrator Kit
Container Type Vial
For Use With For use with Atellica® IM Analyzer
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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  • Atellica® IM SARS-CoV-2 IgG (COV2G) assay is ONLY for use under the Food and Drug Administration’s 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
  • 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
  • Atellica IM 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 Atellica IM 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 Atellica IM SARS-CoV-2 IgG (COV2G) assay may occur due to crossreactivity from pre-existing antibodies or other possible causes
  • Kit includes: 5 ReadyPack® primary reagents, 2 X 1 mL vial low calibrator and 2 X 1 ml vial high calibrator