Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Calibrators / Calibrator / Calibrator Access® SARS-CoV-2 IgG 2 mL For Calibrating the Access SARS-CoV-2 IgG Assay for the in vitro Qualitative Detection of SARS-CoV-2 IgG Antibodies in Human Serum and Plasma (Heparin, EDTA, Citrate) for use on the Access Family of Immunoassay Systems OnlyC58963
Picture of Calibrator Access® SARS-CoV-2 IgG 2 mL For Calibrating the Access SARS-CoV-2 IgG Assay for the in vitro Qualitative Detection of SARS-CoV-2 IgG Antibodies in Human Serum and Plasma (Heparin, EDTA, Citrate) for use on the Access Family of Immunoassay Systems OnlyC58963

Calibrator Access® SARS-CoV-2 IgG 2 mL For Calibrating the Access SARS-CoV-2 IgG Assay for the in vitro Qualitative Detection of SARS-CoV-2 IgG Antibodies in Human Serum and Plasma (Heparin, EDTA, Citrate) for use on the Access Family of Immunoassay Systems OnlyC58963

Calibrator-Access®-SARS-CoV-2-IgG-2-mL-For-Calibrating-the-Access-SARS-CoV-2-IgG-Assay-for-the-in-vitro-Qualitative-Detection-of-SARS-CoV-2-IgG-Antibodies-in-Human-Serum-and-Plasma-(Heparin,-EDTA,-Citrate)-for-use-on-the-Access-Family-of-Immunoassay-Systems-OnlyC58963

SKU #

#1167487

MPN #

C58963

Brand

Beckman Coulter

Stock

In Stock

Quantity

100

Features

CALIBRATOR, ACCESS SARS-COV-2 IGG (1/BX) D/S

$238.40 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1167487
Manufacturer # C58963
Brand Access®
Manufacturer Beckman Coulter
Application Calibrator
Container Type Vial
For Use With For Calibrating the Access SARS-CoV-2 IgG Assay for the in vitro Qualitative Detection of SARS-CoV-2 IgG Antibodies in Human Serum and Plasma (Heparin, EDTA, Citrate) for use on the Access Family of Immunoassay Systems Only
Levels Positive Level / Negative Level
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 41116145
Volume 2 mL
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  • This product has been authorized by FDA under an EUA for use by laboratories certified under CLIA, that meet requirements to perform moderate or high complexity tests: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
  • The Access 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
  • 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 the Access SARS-CoV-2 IgG assay may occur due to cross-reactivity from pre-existing antibodies or other possible causes
  • Provided ready to use
  • Refer to calibration card for exact concentrations
  • For In Vitro Diagnostic Use
  • Rx Only
  • Access SARS-CoV-2 IgG calibrators are provided as: negative and positive