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Haematology Analyser KHA-A100

Haematology Analyser KHA-A100

Overview

Haematology Analyser KHA-A100 is a fully-automated 20 parameter 3-part WBC differentiation benchtop blood cell counter unit. System features color LCD display, large storage memory, error alarms, 2 counting modes for whole blood and prediluted samples. Internal software system detects mechanical failures, enables calibration facility as well as advanced QC testing for standardized operation at reduced routine servicing. System is equipped with back-flush as well as blockage removal facility to improve hygiene control.

Features

  • - 8.4-inch color LCD display
    Throughput: 60 samples/hr
    Performs 20 parameter testing with 3 histogram
    Whole-blood and Pre-diluted modes
    Connectivity options for data transfer
    Stores up to 35000 patient records
    Built-in thermal printer
    External printer (Optional)
Specifications
Type Fully automated 3-part differential system
Throughput 60 samples/hr
Principle of Operation NA
Testing Parameters WBC, LYM#, MON#, GRA#, LYM%,MON%, GRA%, RBC, HGB, MCHC, MCH, MCV, PDW, RDW-CV, RDW-SD, HCT, PLT,MPV, P-LCR, PCT with Histograms for WBC, RBC and PLT.
Accuracy (CV %) WBC (10<sup>9</sup>/L) : 2.0 % (7.0 - 15.0) </br> RBC (10<sup>12</sup>/L) : 1.5 % (3.50 - 6.00) </br> HGB (g/L) : 1.5 % (110 - 180) </br> MCV (fL) : 0.4 % (80.0 - 110.0) </br> PLT (10<sup>9</sup>/L) : 4 % (100 - 500)
Linear Range NA
Sample Mode NA
Test Mode NA
Screen Display 8.4” display color LCD
Resolution 640 x 480
Sample Volume Pre-diluted : 20 µL </br> Whole blood : 9.8 μL
Reagents NA
Aperture Diameter WBC : 80µm </br> RBC : 50µm
Carryover WBC / RBC / HGB <0.5 % PLT<1.0 %
QC NA
Connectivity LAN, USB, RS-232
Printer Built-in Thermal printer
Storage 35,000 records
Operating Temperature 15 °C to 35 °C
Humidity 10 % - 90 %
Maintenance NA
Power Supply AC 110 V – 220 V, 50 / 60 Hz
Dimensions 436 x 363 x 367 mm
Weight 18 Kgs
Applications

Used in diagnostic laboratories, pathological diagnostic centers to characterize blood cells, determine their count and cell volume for in-vitro pathological diagnosis of blood samples to meet qualifying performance requirements and standardized results for multiple sample analysis.

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