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LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm

    Buy cheap LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm from wholesalers
     
    Buy cheap LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm from wholesalers
    • Buy cheap LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm from wholesalers
    • Buy cheap LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm from wholesalers

    LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm

    Ask Lasest Price
    Brand Name : LABNOVATION
    Model Number : LD-100
    Certification : IFCC, NGSP, CE
    Price : Negotiation
    Payment Terms : D/A, D/P, T/T
    Supply Ability : 100/Day
    Delivery Time : 10 work day
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    LD-100 PPOCT HbA1c Auto Hematology Analyzer Machine 220mm*150mm*120mm

    HbA1c Analyzer LD-100 (PPOCT) Fully Automatic HbA1c Testing Analyzer One Step Operation Analyzer

    Intended Use

    • It is one of the Labnovation HbA1c Testing Analyzer
    • Intended for the content determination of hemoglobin A1c (HbA1c) in human whole blood.
    • Testing with 4μL sample,fast testing speed within 3min
    • Color touch screen easy to click and read the results
    • Protable and convience,suitable for the detection of HbA1c in medical units at all levels.

    Specifications

    ModelLD-100
    Measurement Time< 3 minutes
    Sample TypeWhole blood
    Sample Volume4ul
    Data storage7000
    Method(Borate affinity)Fluorescent Immunoturbidimetry
    Operating TypeOne-Step, fully automatic system
    Measurement RangeHbA1c 4.0~15%(NGSP Unit)
    eAG 68-385mg/dl(mmol/l)
    Operating ConditionTemperature:15~35℃
    Humidity:15~80%R.H
    Storage ConditionAnalyzer:10-60℃; Test kit: 2~8℃
    Power connectionDetachable power supply cord
    CertificatedNGSP, IFCC


    Basic Parameters

    • Blood collection volume: The sampling volume of whole blood should not be less than 4μl.
    • Sample volume: 4μl full-blood.
    • Analytical wave-length: 510nm and 580nm.

    Analysis Interface

    Click the Analysis button on the main interface to enter the sample detection program. For details, see 5.3 Sample Detection


    PRINCIPLE

    • Uses the (borate affinity) fluorescent immunoturbidimetry
    • Push a mixture containing a fluorescent borate conjugate into an integrated test cup and mix to dissolve sufficiently.
    • The blood samples in the sample collector are then pushed into the buffer and mixed to release the hemoglobin from the red blood cells.
    • The total concentration of hemoglobin depends on the initial reduced fluorescence signal.
    • Fluorescent borate conjugates bind to glycosylated hemoglobin, and glycosylated hemoglobin is determined by detecting the decrease of fluorescent active ingredients.
    • The percentage of glycosylated hemoglobin in total hemoglobin can be determined.

    Feature

    • Simple Operation Step, One-Step Testing Process
    • Protable, Light and Small,Easy to carry
    • Working environment: Standard
    • Battery Integrated
    • Operating mode: Continuous
    • High Accuracy
    • RFID For Batch Management
    • Color Touch Screen
    • One Analyzer For HbA1c Testing

    Reliable

    IFCC calibratorNormalAbnormalNormalAbnormal
    Mean HbA1c%5.49.65.39.2
    CV (%)2.5%1.9%2.4%1.8%

    Use Step

    • Place cartridge in analyzer
    • Push bead into reagents
    • Insert sample into cartridge


    Performance Indicators

    • Accuracy: tested with the reference material as samples, and the relative deviation of the determination results of the analyzer should be within the range of ±8%.
    • Precision: Samples with a concentration of 4.0%-6.5% are detected, and the sample coefficient of variation (CV) of the test results is within 3%.
    • Linearity:In the range of 4%-16% of HbA1c, the linear correlation coefficient r of the test results should be no less than 0.9900.
    • Stability:Within 8 hours after the instrument is turned on and stable, the same normal sample is tested, and the relative deviation of the test results is not more than ±3%.
    • Permission: The authority is the first-level authority, and the login authority is the first-level authority.

    Certificated


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