Finecare cTnI Rapid Quantitative Test

✅ Key Features & Specifications

• Test principle: Fluorescence Immunoassay (FIA) for the quantitative detection of cardiac troponin I (cTnI) in human whole blood, serum, or plasma.

• Intended use: An aid in the diagnosis of acute myocardial infarction (AMI) and in monitoring patients with suspected cardiac injury or at risk of major adverse cardiac events (MACE).

• Sample types: Whole blood, serum, or plasma.

• Sample volume: Approximately 75 µL (serum/plasma) or 100 µL (whole blood) per test.

• Turnaround time: Results available in about 15 minutes.

• Measurement range: Typically 0.1 ng/mL to 50 ng/mL.

• Storage conditions: Cartridges stable at 4 °C – 30 °C, with a shelf life of up to 24 months.

• Instrument compatibility: Requires a Finecare™ Fluorescence Immunoassay Analyzer (e.g., Finecare, Finecare Plus, or Finecare II) for quantitative result reading.