Haematology Analyser KHA-B100

Haematology Analyser KHA-B100

Haematology Analyser KHA-B100 is a fully-automated 28 parameter 5-part WBC differentiation benchtop blood cell counter unit. System adopts 3D topographic WBC mapping to illustrate different properties of WBC. Integrated Ti incubation system ensures constant temperature for accurate 5-part differentiation. Multiple QC protocols and calibration function allows standardized operation. User-oriented software provides large data storage, alarms, LIS interface, flexible data management system with versatile formats.

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Type Fully automated 5-part differential system
Throughput 60 samples/hr
Principle of Operation N/A
Testing Parameters WBC, RBC, HGB. HCT, MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, PDW, MPV, PCT, P-LCR, NEU#, NEU%, LYM#, LYM%, MON#, MON%, EOS#, EOS%, BAS#, BAS%, ALY#, ALY%, IG#, IG%, 2 histograms, 2 scatter grams.
Accuracy (CV %) WBC (109/L) : 2.0 %
RBC (1012/L) : 1.5 %
HGB (g/L) : 1.5 %
PLT (109/L) : 4 %
Linear Range WBC (109/L) : 1.0 – 99.9
RBC (1012/L) : 0.3 – 7.0
HGB (g/L) : 20 – 24
PLT (109/L) : 20 – 999
Sample Mode Pre-diluted
Whole blood
Test Mode CBC+5DIFF test
CBC test
Screen Display N/A
Resolution N/A
Sample Volume N/A
Reagents N/A
Aperture Diameter N/A
Carryover WBC / RBC / HGB <0.5 % PLT<1.0 %
QC N/A
Connectivity LIS interface with HL7
Printer Built-in Thermal printer
Storage 1,00,000 records
Operating Temperature 15 °C to 30 °C
Humidity 30 % - 85 %
Maintenance N/A
Power Supply AC 110 V – 220 V, 50 / 60 Hz
Dimensions 460 x 570 x 610 mm
Weight 53 Kgs
  • • Flow Cytometry technology
  • • Continuous linear shealth flow technique
  • • Non-toxic reagents
  • • Desktop for display and user interface
  • • Throughput: 60 samples/hr
  • • Performs 28 parameter testing with 2 histogram and 2 scatter gram
  • • Whole-blood and Pre-diluted sample modes
  • • CBC+Diff and CBC test modes
  • • Stores up to 1, 00, 000 patient records
  • • Built-in thermal printer
  • • External printer (Optional)

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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