Dry Fluorescence Immunoassay Analyzer | Rapid POCT Diagnostic System

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Portable Dry Fluorescence Immunoassay Analyzer for rapid, quantitative POCT diagnostics. Detects cardiac markers, hormones, and inflammatory agents with high accuracy using Europium conjugation....


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    Advanced Dry Fluorescence Immunoassay (FIA) Diagnostic System

    The Dry Fluorescence Immunoassay Analyzer is a state-of-the-art Point-of-Care Testing (POCT) platform designed for rapid, accurate, and quantitative detection of a vast range of biomarkers. By utilizing the principle of photoelectric detection combined with advanced Europium (Eu3+) conjugation technology, this system bridges the gap between laboratory-grade precision and bedside convenience.

    Its compact, portable design makes it an ideal choice for diverse medical settings, including emergency rooms, intensive care units (ICU), outpatient clinics, and community health centers.

    System Excellence & Technology

    • High Sensitivity: The Europium-based reagents provide superior fluorescence stability and a wide dynamic range, ensuring high analytical sensitivity even for low-concentration markers like cTnI or AMH.

    • Broad Diagnostic Menu: A single analyzer supports multiple clinical panels, including Cardiac Markers, Inflammatory Markers, Fertility Hormones, Anemia, and Gastric Tumor Markers.

    • Rapid Turnaround Time (TAT): Most tests provide quantitative results within 3 to 15 minutes, significantly accelerating clinical decision-making.

    • Ease of Operation: The user-friendly interface and simple procedure (Apply Sample → Insert Card → Read Result) require minimal specialized training.

    • Portable & Robust: Small footprint with dependable photoelectric performance, suitable for near-patient testing in all laboratory environments.


    Fluorescence Immunoassay Pane


    CategoryTest ItemsSpecimen TypeSample VolumeReaction TimeDetection Range
    Bone / FertilityVitamin DWB/S/P100 μL15 mins10-70 ng/mL

    β-HCGWB/S/P20 μL15 mins2-200,000 mIU/mL

    FSH / LHWB/S/P100 μL15 mins1-100 mIU/mL

    AMHWB/S/P80-160 μL15 mins0.1-16 ng/mL
    Cardiac MarkersNT-ProBNPWB/S/P100 μL15 mins30-30,000 pg/mL

    cTnIWB/S/P75 μL15 mins0.1-50 ng/mL

    cTnI/Myo/CK-MBWB/S/P100 μL15 minscTnI: 0.1-32 ng/mL
    ThrombusD-DimerWB/P15-30 μL5 mins0.1-10 mg/L
    InflammatoryPCTWB/S/P100-200 μL15 mins0.1-100 ng/mL

    CRP / SAAWB/S/P10-20 μL3-5 minsCRP: 0.5-200 mg/L
    Tumor (Gastric)PGI / PGIIWB/S/P100 μL15 minsPGI: 2.5-200 ng/mL
    AnemiaFerritin / Vit B12WB/S/P60-120 μL10-15 mins5-500 ng/mL


    1. What is a Dry Fluorescence Immunoassay Analyzer used for?It is a POCT device used for the rapid, quantitative detection of various analytes, including cardiac markers, hormones, and inflammatory proteins in human blood samples.

    2. How does the Europium conjugation principle improve test accuracy?Europium-based fluorescence offers a larger Stokes shift and longer fluorescence life, which minimizes background noise and significantly increases the sensitivity and accuracy of the assay.

    3. What specimen types can the FIA system process?The system is highly versatile, supporting Whole Blood (WB), Serum (S), and Plasma (P) for most test items, making it suitable for both clinical and emergency use.

    4. Which cardiac markers can be detected using this analyzer?The analyzer supports a comprehensive cardiac panel, including NT-ProBNP, cTnI, Myoglobin, CK-MB, BNP, cTnT, and H-FABP.

    5. Is there a multi-parameter test available for chest pain diagnosis?Yes, we offer a 3-in-1 cTnI/Myo/CK-MB combo panel that provides simultaneous quantitative results from a single 100 μL sample.

    6. How fast can I get a D-Dimer result?Our rapid D-Dimer assay provides quantitative results in just 5 minutes, which is critical for the rapid exclusion of venous thromboembolism.

    7. What is the detection range for the high-sensitivity CRP test?The CRP test has a wide detection range from 0.5 mg/L to 200 mg/L, covering both conventional inflammation and high-sensitivity (hs-CRP) applications.

    8. Can the system be used for fertility and ovarian reserve assessment?Yes, the system accurately detects AMH (0.1-16 ng/mL) for ovarian reserve, along with FSH, LH, and β-HCG for comprehensive fertility monitoring.

    9. What gastric tumor markers are supported?The system supports the "Gastric Function" panel, including Pepsinogen I (PGI), Pepsinogen II (PGII), and Gastrin-17 (G-17) for gastric mucosal screening.

    10. Does the analyzer require complex maintenance?No, the dry immunoassay system is designed for minimal maintenance with no liquid pathways to clean, making it more stable than traditional wet chemistry systems.

    11. What are the sample volume requirements?Sample volumes are micro-scale, ranging from as little as 10 μL (for CRP/SAA) up to 200 μL, depending on the specific test item and specimen type.

    12. Is the FIA system CE certified for professional laboratory use?Yes, our diagnostic system and reagents are manufactured under ISO 13485 and are CE approved for professional in vitro diagnostic (IVD) use.

    13. Can the results be exported to a hospital LIS/HIS system?Most modern FIA analyzers support standard data connectivity options for seamless integration with Laboratory Information Systems (LIS).

    14. How should the FIA reagents be stored?The dry reagents are typically stable at room temperature or refrigerated (depending on the specific item), ensuring a long shelf life and cost-effectiveness.

    15. Does the system support Vitamin B12 and Ferritin testing for anemia?Yes, it provides quantitative results for both Vitamin B12 and Ferritin, assisting in the rapid diagnosis of different types of anemia.


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