Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Calibrators / Calibrator Kit / Calibrator Kit Abbott SARS-CoV-2 IgG 1 X 2.0 mL For the Calibration of the Architect i System when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma06R8601
Picture of Calibrator Kit Abbott SARS-CoV-2 IgG 1 X 2.0 mL For the Calibration of the Architect i System when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma06R8601

Calibrator Kit Abbott SARS-CoV-2 IgG 1 X 2.0 mL For the Calibration of the Architect i System when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma06R8601

Calibrator-Kit-Abbott-SARS-CoV-2-IgG-1-X-2-0-mL-For-the-Calibration-of-the-Architect-i-System-when-used-for-the-Qualitative-Detection-of-IgG-Antibodies-to-SARS-CoV-2-in-Human-Serum-and-Plasma06R8601

SKU #

#1164347

MPN #

06R8601

Brand

Abbott

Stock

In Stock

Quantity

100

Features

CALIBRATOR, ARCH SARS-COV-2 IGG D/S

$99.00 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1164347
Manufacturer # 06R8601
Brand Abbott
Manufacturer Abbott
Application Calibrator Kit
For Use With For the Calibration of the Architect i System when used for the Qualitative Detection of IgG Antibodies to SARS-CoV-2 in Human Serum and Plasma
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Storage Requirements Requires Refrigeration
Test Name SARS-CoV-2 IgG
Test Type Antibody Test
UNSPSC Code 41116128
Volume 1 X 2.0 mL
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  • The SARS-CoV-2 IgG 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
  • The SARS-CoV-2 IgG 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
  • Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C 263a, to perform moderate or high complexity test
  • Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities
  • 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 SARS-CoV-2 IgG assay may occur due to cross-reactivity from pre-existing antibodies or other possible causes
  • Contains inactivated, cell-free, human blood-derived material, reactive for anti-SARS-CoV-2 IgG
  • Preservatives: sodium azide and antimicrobial agents
  • Prescription Use only; For In Vitro Diagnostic Use Only