Home / Clinical Laboratory / Clinical Analyzer Calibrators and Reagents / Reagents / Reagent Kit / Reagent Kit Dimension® EXL™ Antibody Test SARS-CoV-2 IgG For Dimension® EXL™ Integrated Chemistry System with LOCI® Module 480 Tests11417770
Picture of Reagent Kit Dimension® EXL™ Antibody Test SARS-CoV-2 IgG For Dimension® EXL™ Integrated Chemistry System with LOCI® Module 480 Tests11417770

Reagent Kit Dimension® EXL™ Antibody Test SARS-CoV-2 IgG For Dimension® EXL™ Integrated Chemistry System with LOCI® Module 480 Tests11417770

Reagent-Kit-Dimension®-EXL™-Antibody-Test-SARS-CoV-2-IgG-For-Dimension®-EXL™-Integrated-Chemistry-System-with-LOCI®-Module-480-Tests11417770

SKU #

#1184489

MPN #

11417770

Brand

Siemens

Stock

In Stock

Quantity

100

Features

REAGENT, DIMENSION CV2G ASSAY (480TEST/KT) D/S

$3,472.43 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 1184489
Manufacturer # 11417770
Brand Dimension® EXL™
Manufacturer Siemens
Application Reagent Kit
Container Type Cartridge
For Use With For Dimension® EXL™ Integrated Chemistry System with LOCI® Module
Form Liquid
Number of Tests 480 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 41116010
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  • The Dimension® EXL™ SARS‑CoV‑2 IgG (CV2G) 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 (CLIA) of 1988, 42 U.S.C 263a, that meet requirements to perform moderate or high complexity tests
  • The Dimension® EXL™ SARS‑CoV‑2 IgG (CV2G) assay is a chemiluminescent immunoassay intended for qualitative and semiquantitative detection of IgG antibodies to SARS‑CoV‑2 in human serum and plasma (dipotassium EDTA and lithium heparin) using the Dimension® EXL™ integrated chemistry system with LOCI® Module
  • Laboratories within the United States and its territories are required to report all results to the appropriate public health authorities
  • The sensitivity of the Dimension® EXL™ SARS‑CoV‑2 IgG (CV2G) 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 Dimension® EXL™ SARS‑CoV‑2 IgG (CV2G) assay may occur due to cross-reactivity from pre-existing antibodies or other possible causes
  • Results are for the detection of SARS‑CoV‑2 IgG antibodies; IgG antibodies to SARS‑CoV‑2 are generally detectable in blood several days after initial infection, although the duration of time antibodies are present post‑infection is not well characterized
  • Dimension EXL CV2G Flex Reagent Cartridge: 8 X 60 Tests