Automatic Fluorescence 5-Part Hematology Analyzer CBC CRP SAA DIFF RET

Automatic Fluorescence 5-Part Hematology Analyzer CBC CRP SAA DIFF RET
Automatic Fluorescence 5-Part Hematology Analyzer CBC CRP SAA DIFF RET
Automatic Fluorescence 5-Part Hematology Analyzer CBC CRP SAA DIFF RET
Automatic Fluorescence 5-Part Hematology Analyzer CBC CRP SAA DIFF RET
PM-E631
Point of origin
ISO13485
Testing item
CBC CRP SAA DIFF RET
Throughput
100T/H
Application scenarios
lab,science,hospital,CDC
Sample
blood

The PM-E631 Automatic Fluorescence 5-Part Hematology Analyzer with CRP & SAA PHeMA-4DS Analysis Technology is a high-precision clinical laboratory device used for detailed blood cell counts, differentials, and inflammatory marker measurements. It is designed to provide comprehensive and accurate hematological analysis.

Specifications

  1. PHeMA-4DS Analysis Technology:

    • Ensures accurate WBC results by preventing interference from lipid particles and fragments.

    • Combines panoramic hematological morphological analysis and four-dimensional scanning.

  2. Low WBC Mode:

    • Triples particle counting for low leukocyte samples to ensure result accuracy.

  3. Cell Detection and Differentiation:

    • RBC and Reticulocyte Detection: Accurate analysis of red blood cells and reticulocytes.

    • WBC Differentiation: Differentiates WBCs into 5 parts, flags significant abnormalities such as immature granulocytes, left shift, and atypical lymphocytes.

  4. PLT Counting Channels:

    • Utilizes impedance method (PLT-I) and fluorescence method (PLT-O).

    • Automatic correction of PLT-I counting result using PLT-O mode.

  5. Fluorescence Detection Technique:

    • Enhances accuracy in differentiating cell types.

  6. High Throughput:

    • Capable of processing 100 tests per hour.

  7. Wide Range CRP and SAA Detection:

    • Uses latex-enhanced immunoscattering turbidimetry.

    • Environmentally friendly cyanide-free detection method.

  8. Multi-dimensional Analysis:

    • WBC/NRBC/RET: Utilizes laser scattering and nucleic acid fluorescence staining.

    • RBC/PLT: Employs sheath flow impedance technology.

    • 38 reporting parameters, including various scatter plots and histograms for detailed analysis.

  9. Sample Types:

    • Compatible with venous whole blood, peripheral whole blood, pre-diluted blood, and serum (for immune items).

  10. Reagents:

    • Includes dilution solutions, RET diluent, dye solutions (RET dye, DIFF dye, NRBC dye), hemolytic agents (DIFF and HGB hemolytic agents, NRBC hemolytic agent), immunoturbidimetric reagent, and probe cleaning solution.


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Clinical Applications

  • Routine Hematology Testing: Provides comprehensive blood cell counts and differentials.

  • Inflammatory Marker Detection: Measures CRP and SAA levels, important for diagnosing inflammatory conditions.

  • Anemia and Hemoglobinopathy Diagnosis: Detects and quantifies red blood cells and reticulocytes.

  • Thrombocytopenia Evaluation: Differentiates and counts platelets using dual methods.

  • Infection and Immune Status Monitoring: Analyzes WBC differentials to identify infections and immune responses.

  • Reticulocyte Count for Bone Marrow Function: Assesses reticulocyte levels for bone marrow activity.

Features

  • Advanced Detection Technology: Ensures accurate and reliable results with minimal interference.

  • High Throughput: Enhances laboratory efficiency with the ability to process 100 tests per hour.

  • Comprehensive Analysis: Provides detailed reporting with multiple scatter plots and histograms.

  • Environmentally Friendly Methods: Uses cyanide-free techniques for safer testing.

  • Versatile Sample Handling: Accommodates various blood sample types for flexibility in testing.


Key technologiesLaser flow cytometry, sheath impedance technology, colorimetry
Detection light sourceSemiconductor laser
WBC/Baso detection methodPanoramic hematology morphology analysis and four-dimensional scanning technology (PHeMA-4DS)
Red blood cell and platelet detection principleSheath impedance method/optical method
HGB detection methodEnvironmentally friendly cyanide-free HGB measurement
CRP detectionImmunoscattering turbidimetry
Detection mode10 measurement modes (CBC, CBC+DIFF, CBC+DIFF+RET, RET, CBC+RET, CBC+DIFF+CRP, CBC+DIFF+CRP+SAA, CRP+SAA, CRP, SAA)
Report parameters38 report parameters
Research parameters19 research parameters
Image parameters3 three-dimensional scatter plots (DIFF, WNR, RET), 8 two-dimensional scatter plots (3 DIFF plots, 3 WNR plots, 2 RET plots), 3 histograms (WNR, RBC, PLT)
Specimen modeStatic Pulse whole blood, peripheral whole blood, pre-diluted blood, serum (for immune items)
PrecisionWBC: (3.5-15) × 109/L, CV ≤ 2.0%
RBC: (3.5-8) × 1012/L, ≤ 1.5%
HGB: (100-180) g/l, ≤ 1%
MCV: (70-120) fl, ≤ 1%
HCT: (35-50)%, ≤ 1.5%
PLT: (100-500) × 109/L, ≤ 4%
CRP: ≤ 10mg/L, SD ≤ 0.5mg/L; > 10mg/L, CV ≤ 4%
Required sample volumeWhole blood mode: ≤ 60μL (CBC + DIFF), ≤ 30μL (CBC); pre-dilution mode: ≤ 20μL
Micro blood testMicro blood collection tube seat
Injection methodManual closure, automatic injection
Loading volume70 samples


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