Chemiluminescent Immunoassay Analyzer LCIA-T2010

Introduction

Chemiluminescent Immunoassay Analyzer uses magnetic particle separation technology. The maximum speed analyzer can offer is 180 T/hr. Its excellent performance is contributed by tubular enzymatic chemiluminescence. Faster reaction and great efficiency are assured by the system. Compact and simplified design for ease of operation. 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

Chemiluminescent Immunoassay Analyzer is used widely for biochemical analysis across biotechnology, medical laboratories, hospitals, veterinary diagnostics, research and academics.

Specifications

Throughput	180 T/H
Principle	Magnetic particle enzymatic chemiluminescence
Operation modes	Random, Batch and
Separation method	Magnetic separation technology
Sample Positions	60 (Each position could be used as an emergency position)
Reagent Positions	25 pcs (2-8 ℃ refrigeration)
Incubation Positions	58
1st Result Time	18 minutes
Sample Volume	10-200 μl
Detection Precision	CV ≤ 5%
Carry-over Rate	≤ 10-5
Correlation Coefficient	r ≥ 0.99
Calibration Stability	28 Days
Calibration Type	6 / 7-point calibration
Software	Windows 7/8/10, 32 or 64 bit, Bi-direction, support HL7 protocol, Intuitive User Interface, Intelligent Data Management
Interface	/IP Network interface
Functions	Liquid level detection, Anti-collision function, Sample barcode scanning, Reagent radio frequency identification, Intelligent alarm prompt.
Power Supply	AC 110/220 V, 50/60 Hz
Exterior Dimension (W × D × H)	768 × 771 × 568 mm
Packaging Dimension (W × D × H)	1303 × 873 × 854 mm
Net Weight	94 Kg
Gross Weight	163 Kg

Features

Safety alarms ensure smooth functioning

Wizard visual interface

Sample integrity is well maintained

Reaction vessels can be added by pouring

Triple magnetic separation cleaning technology

Forced air cooling reagent tray

Real time updating of detection process

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.