Hematology Analyzer LHTA-T2010

Introduction

Hematology Analyzer can process up to 60 samples per hour. It requires only 12μl for whole blood and 20μl for pre-diluted blood samples for testing. Offers an analysis of 21 parameters along with 3 histograms. Featuring a 9.7-inch color touch detection of . This medical equipment is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.

Applications

Hematology analyzers provide detailed information on complete blood count () analysis and hemoglobin analysis. It is utilized across clinical laboratories, hematology clinics, veterinary medicine, pharmaceutical research, and biotechnology sectors.

Specifications

Throughput	60 samples/hour
Channels	2
Histograms	3 histograms (including , , histograms)
Sample Volume	Whole blood: 12 µl Pre-diluted: 20 µl
Calibration	Manual, auto-calibration
Counting Modes	Venous, capillary, pre-diluted
Printing Model	Auto print, manual print
Principle	Impedance for differentiation and // count; Colorimetric method for
Parameters	21 parameters (including , Mid%, Lym%, Gran%, Mid%, Lym%, Gran%, , , , , , , -SD, -CV, , , , , , P-)
Interface	Support Bi-Directional
Language	English, Spanish, French, Russian, Ukrainian
Reagent	Diluent 10L, Hemolytic agent 250 ml, Probe cleanser 50 ml
Data Input	9.7-inch touch screen, mouse, keyboard (optional)
Output	Internal printer, support external printer
Printer Paper Size	57 × 30mm
Interface	4 ports, network port, RS232 serial port
Storage	100,000 results with histogram
Unclog	High voltage burns, reverse high-pressure flush
Working Temperature	15℃ to 30 ℃
Relative Humidity Range	30% to 85%
Atmospheric Pressure Range	70.0 kPa to 106.0 kPa
Carry-Over Rate	: ≤ 1.5% : ≤ 1% : ≤ 1% : ≤ 3%
Background	≤ 0.3× 10⁹/L ≤ 0.03 × 10¹²/L ≤ 1g/L ≤ 5.0% ≤ 10×10⁹ /L
Linearity	Parameter Measurement Range CV (0.5~10.00×10⁹)/L, (10.10~99.9×10⁹)/L (±0.5×10⁹)/L, ±5% (0.05~1.00×10¹²)/L, (1.01~9.99×10¹²)/L (±0.05×10¹²)/L, ±5% (2~70g)/L, (71~300.0g)/L (±2.0g)/L, ±2% (10~100×10⁹)/L, (101~999×10⁹)/L (±10.0×10⁹)/L, ±8%
Precision	Parameter Repeatability Measurement range ≤ 6.0% (3.5 to 9.5 × 10⁹)/L ≤ 3.0% (3.8 to 5.8 × 10¹²)/L ≤ 2.5 % (115 to 175g)/L ≤ 10.0 % (125 to 350 × 10⁹)/L ≤ 3.0 % 35% to 50%
Power Supply	100-240 AC, 50/60Hz, 150VA
Reagent Dimension	340 × 340 × 340 mm
External Dimension (W×D × H)	295 × 467 × 418 mm
Packaging Dimension (W × D × H)	404 × 564 × 616 mm
Reagent Weight	13 Kg
Net Weight	19 Kg
Gross Weight	31 Kg

Features

Built-in thermal printer

External printers can be connected

Operates 24 hours

Fully intelligent blockage removal

Alarm functions available

Automatic and manual calibration modes

Supports system

FAQs

1. What are the key factors to consider when selecting this medical equipment for laboratory use?

When selecting this medical equipment, key factors include: 1) The instrument's precision and accuracy to meet experimental requirements; 2) Compatibility with the types of samples and applications you will be working with; 3) Ease of use and maintenance requirements; 4) Safety features to protect operators and samples; 5) Calibration and certification requirements; 6) Cost-effectiveness and long-term reliability; 7) Technical support and service availability from the supplier. Evaluating these factors ensures that the instrument meets your laboratory's specific needs.

2. How often should this medical equipment be calibrated to ensure accurate results?

It is recommended to calibrate this medical equipment at least once every 6-12 months under normal usage conditions. More frequent calibration (every 3-6 months) may be necessary if: 1) The instrument is used continuously for extended periods; 2) It is exposed to harsh environmental conditions (temperature fluctuations, humidity, dust); 3) It is used for critical applications requiring high precision; 4) The instrument has been moved or subjected to physical shock; 5) Calibration checks indicate significant deviations from standard values. Always follow the manufacturer's calibration guidelines.

3. What are the common maintenance procedures required for this medical equipment?

Common maintenance procedures include: 1) Regular cleaning of the instrument's exterior and sample contact surfaces to prevent contamination and ensure proper operation; 2) Inspection of moving parts (if applicable) for wear and lubrication as recommended by the manufacturer; 3) Replacement of consumable parts (filters, bulbs, reagents) according to usage guidelines; 4) Verification of performance parameters (temperature, pressure, voltage) regularly; 5) Storage of the instrument in a clean, dry environment when not in use; 6) Keeping a maintenance log to track service activities and identify potential issues early; 7) Following the manufacturer's specific maintenance schedule for optimal performance and longevity.

4. Can this medical equipment be used with different types of samples, and are there any compatibility considerations?

Yes, this medical equipment can be used with a variety of sample types, but compatibility considerations are important: 1) Check if the instrument's materials are compatible with the chemical composition of your samples (avoid corrosive or reactive substances that may damage the instrument); 2) Ensure that the sample volume and concentration are within the instrument's recommended range; 3) For biological samples, consider sterility requirements and potential cross-contamination risks; 4) For volatile or hazardous samples, ensure proper ventilation and safety precautions are in place; 5) Consult the manufacturer's documentation for specific sample compatibility guidelines, and perform compatibility tests with new sample types before regular use.

5. What should be done if the medical equipment malfunctions or produces inconsistent results?

If malfunctions or inconsistent results occur: 1) First, check the instrument's user manual for troubleshooting guidelines specific to the issue; 2) Verify that the instrument is properly calibrated and within its calibration period; 3) Inspect for obvious issues such as loose connections, damaged parts, or incorrect settings; 4) Clean the instrument thoroughly to remove any contamination that may affect results; 5) Repeat the experiment with a known standard sample to determine if the issue is with the instrument or the sample; 6) If the problem persists, discontinue use of the instrument to prevent further damage or inaccurate results; 7) Contact technical support or a qualified service technician for diagnosis and repair, providing details of the issue and any troubleshooting steps already performed.