-
,for, Item ID-
- #1203249
- Siemens #11207300
Immunoassay Reagent / Calibrator Kit Advia Centaur® Enhanced Liver Fibrosis (ELF) For Advia Centaur XP / Centaur XPT Immunoassay Systems 50 Tests
REAGENT, CENTAUR ELF ADVID (5 0/BX)
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Features
- ADVIA Centaur® Enhanced Liver Fibrosis (ELF™) is for in vitro diagnostic use in the determination of an ELF score based on the combined quantitative measurements of hyaluronic acid, amino‑terminal propeptide of type III procollagen, and tissue inhibitor of matrix metalloproteinase 1 in human serum using the ADVIA Centaur® XP and ADVIA Centaur® XPT systems
- ADVIA Centaur ELF is indicated as a prognostic marker in conjunction with other laboratory findings and clinical assessments in patients with advanced fibrosis (F3 or F4) due to non‑alcoholic steatohepatitis (NASH) to assess the likelihood of progression to cirrhosis and liver-related clinical events
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Product Specifications
McKesson # | 1203249 |
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Manufacturer # | 11207300 |
Brand | Advia Centaur® |
Manufacturer | Siemens |
Country of Origin | United States |
Application | Immunoassay Reagent / Calibrator Kit |
For Use With | For Advia Centaur XP / Centaur XPT Immunoassay Systems |
Number of Tests | 50 Tests |
Product Dating | McKesson Acceptable Dating: we will ship >= 90 days |
Sample Type | Serum Sample |
Specialty | Immunoassay |
Test Category | Liver Disease |
Test Method | 2‑Site Sandwich Assay |
Test Name | Enhanced Liver Fibrosis (ELF) |
Test Type | Hepatic |
UNSPSC Code | 41116004 |
Volume | Lite Reagent: 10 mL, Solid Phase: 10 mL, Ancillary Well Reagent: 5 mL |
Features
- ADVIA Centaur® Enhanced Liver Fibrosis (ELF™) is for in vitro diagnostic use in the determination of an ELF score based on the combined quantitative measurements of hyaluronic acid, amino‑terminal propeptide of type III procollagen, and tissue inhibitor of matrix metalloproteinase 1 in human serum using the ADVIA Centaur® XP and ADVIA Centaur® XPT systems
- ADVIA Centaur ELF is indicated as a prognostic marker in conjunction with other laboratory findings and clinical assessments in patients with advanced fibrosis (F3 or F4) due to non‑alcoholic steatohepatitis (NASH) to assess the likelihood of progression to cirrhosis and liver-related clinical events
More Information
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