Home / Clinical Laboratory / Controls / Master Curve Material / Antibody Test Master Curve Material Atellica® IM SARS-CoV-2 IgG Level 1, 2, 3, 4 4 X 1 mL11207587
Picture of Antibody Test Master Curve Material Atellica® IM SARS-CoV-2 IgG Level 1, 2, 3, 4 4 X 1 mL11207587

Antibody Test Master Curve Material Atellica® IM SARS-CoV-2 IgG Level 1, 2, 3, 4 4 X 1 mL11207587

Antibody-Test-Master-Curve-Material-Atellica®-IM-SARS-CoV-2-IgG-Level-1,-2,-3,-4-4-X-1-mL11207587

SKU #

#1185713

MPN #

11207587

Brand

Siemens

Stock

In Stock

Quantity

100

Features

CONTROL, ATELLICA IM SARS-COV-2 IGG 4X1ML (4/KT) D/S

$795.64 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1185713
Manufacturer # 11207587
Brand Atellica® IM
Manufacturer Siemens
Application Master Curve Material
Container Type Vial
For Use With For Verification of Calibration and Measuring Interval of the Atellica® IM SARS-CoV-2 IgG (sCOVG) Assay
Levels Level 1, 2, 3, 4
Product Dating McKesson Acceptable Dating: we will ship >= 30 days
Storage Requirements Requires Refrigeration
Test Name SARS-CoV-2 IgG
Test Type Antibody Test
UNSPSC Code 41116145
Volume 4 X 1 mL
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  • The Atellica IM SARS-CoV-2 IgG is for use under Emergency Use Authorization Only: https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-serology-and-other-adaptive-immune-response-tests-sars-cov-2
  • 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 Atellica® IM SARS-CoV-2 IgG Master Curve Material (sCOVG MCM) is for in vitro diagnostic use in the verification of calibration and measuring interval of the Atellica® IM SARS-CoV-2 IgG (sCOVG) assay
  • Negative results do not preclude acute SARS-CoV-2 infection; if acute infection is suspected, direct testing for SARS-CoV-2 is necessary
  • Results from antibody testing should not be used to diagnose or exclude acute SARS-CoV-2 infection
  • Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities