The ADVIA Centaur TnI-Ultra assay presented high reproducibility and high sensitivity. The use of the recommended lower cutpoint ( microg/L) implied an increased and earlier identification of www.doorway.ru by: Take a virtual tour of the ADVIA Centaur XP Immunoassay System. High throughput, up to tests/hour. Intuitive software for ease of operation. STAT port guarantees priority sampling at any time. Data archive reduces administrative tasks. Extensive menu with 30 onboard reagents. · Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay. In-Vitro Diagnostic for quantitative determination of cardiac troponin For in vitro diagnostic use in the quantitative determination of cardiac.
ADVIA Centaur Tni-Ultra Assay; SMN - tests and SMN tests Product Usage: For in vitro diagnostic use in the quantitative determination of cardiac troponin I (cTnl) in serum, heparinized plasma, or EDTA plasma using the ADVIA Centaur/ADVIA Centaur XP/ADVIA Centaur XPT/ADVIA Centaur CP systems. Advia Centaur cTnI (within-run CV as established. with a CLSI evaluation protocol at a concentration of. Centaur Assay Manual [on] TnI-Ultra. , Rev. A, This is a printed. In addition, cTnI-Ultra concentration was determined in EDTA-preserved plasma using the ADVIA Centaur TnI-Ultra assay. This 3-site sandwich immunoassay uses direct chemiluminometric technology. An ancillary reagent is included to reduce nonspecific binding.
ADVIA Centaur XPT TNIH1 ADVIA Centaur XPT TnI-Ultra™6 Comparison of number of subjects with undetectable troponin Since clinical data were not available, comparisons between the ADVIA Centaur TNIH assay and the other assay at each site were performed for the number of subjects with values below the respective LoDs, and below the respective 99th. The ADVIA Centaur TnI-Ultra assay presented high reproducibility and high sensitivity. The use of the recommended lower cutpoint ( microg/L) implied an increased and earlier identification of MI. ADVIA Centaur® TnI-Ultra Assay ADVIA Centaur® TnI-Ultra Calibrators G. Regulatory Information: 1. Regulation section: 21 CFR , Immunoassay method, troponin subunit 21 CFR , Calibrator, Secondary 2. Classification: Class II 3. Product code: MMI JIT.
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