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Generate Catalog For :
Haematology Analyser KHA-B100
Download Catalog
Personalized PDF Catalog
Catalog Generated On :
22/12/2024
Haematology Analyser KHA-B100
Description :
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.
Specifications :
Type
Fully automated 5-part differential system
Throughput
60 samples/hr
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
Carryover
WBC / RBC / HGB <0.5 %
PLT<1.0 %
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 %
Power Supply
AC 110 V – 220 V, 50 / 60 Hz
Dimensions
460 x 570 x 610 mm
Weight
53 Kgs
Features :
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)
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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