LIODetect® Troponin I
| Product Type: | In Vitro Diagnostic (IVD) |
|---|---|
| Technology: | Lateral Flow |
| Sample Type: | Whole Blood, Serum, Plasma |
| Intended Use: | POCT and laboratory |
| Certifications: | ISO 13485 |
| Manufacturing: | Germany |
LIODetect® Troponin I is a lateral flow immunochromatographic assay for qualitative detection of cardiac troponin I (cTnI) in human whole blood, serum, or plasma. cTnI is a key biomarker for early assessment of myocardial injury and acute coronary syndrome.
The test provides results in 10-15 minutes and is manufactured and quality-controlled in Germany under ISO 13485 standards.
Assay Principle
LIODetect® Troponin I uses lateral flow immunochromatography: cTnI in the sample binds to immobilized anti-cTnI antibodies on the test strip. Migration along the membrane generates visible lines indicating presence of troponin I, while a control line confirms proper test performance.
Intended Use
The assay is intended for professional in vitro diagnostic use in point-of-care testing (POCT) and laboratory settings to support early detection of myocardial injury. Results must be interpreted alongside clinical examination, patient history, and other diagnostic tests.
Test Kit Components
- Individually packaged test strips
- Sample buffer
- Capillary or dropper for sample application
- Instructions for Use (IFU)
Technical Specifications
- Sample material: Whole blood, serum, or plasma
- Technology: Lateral flow immunochromatography
- Time to result: 10-15 minutes
- Result: Qualitative
- Storage conditions: See IFU
- Kit formats: Multiple sizes available
Documents & Regulatory Information
Regulatory status and product availability may vary by country. See official documentation for details.
Quote / Order
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