Introduction
An auto chemistry analyzer is a clinical chemistry analyzer with the automatic operation, used for the measurement of the biochemical parameters in the blood and the other biological samples, and it is used in the clinical, the medical, the research, and the many other applications. The auto chemistry analyzer measures the parameters, such as the glucose, the cholesterol, the proteins, the enzymes, and the electrolytes, by the photometric and the other methods, with the automatic sample and the reagent handling and the automatic measurement; the auto chemistry analyzer consists of a sample handling system, a reagent system, a reaction and a measurement system, a control and a data system, and the display, and it processes the samples in the batches, with features such as the automation and the data management; the auto chemistry analyzer is used for the clinical chemistry tests, for the measurement of the metabolic parameters, for the monitoring of the diseases, for the screening, for the research, and for many other applications, and it is an essential instrument in the clinical laboratory. Auto chemistry analyzers are used in the clinical laboratories, in the hospitals, in the medical, in the research, and for many other applications. With their automatic operation, auto chemistry analyzers are essential for the efficient clinical testing.
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Standards
IEC 61010-2-081:2015-Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes
Complies with the above standards, but is not limited to them.
Features
1. Auto chemistry analyzer for automated clinical chemistry testing.
2. High-throughput analysis of blood, serum and plasma for diagnostic parameters.
3. Suitable for hospitals, clinical laboratories, diagnostic centers and research.
4. Includes sample handler, reagent system, optics, software and operation manual.
5. Supports automated analysis of liver, kidney, lipid, glucose and electrolytes.
FAQ
Q1: What testing scenarios is this analyzer mainly applied to?
A: The auto chemistry analyzer is used in hospitals, clinical laboratories, diagnostic centers, research institutions and healthcare facilities to perform automated clinical chemistry testing of blood, serum and plasma samples for diagnostic parameters including liver function, kidney function, lipid profile, glucose, electrolytes, proteins and enzymes. It supports routine clinical chemistry testing for patient diagnosis and monitoring, high-throughput hospital laboratory testing, health screening panels, metabolic disease monitoring, pharmaceutical clinical trials, and research laboratory analysis. The automated system provides consistent, reproducible results with high throughput, reducing operator variability and supporting efficient clinical laboratory operations.
Q2: What standards does the analyzer comply with?
A: The auto chemistry analyzer complies with relevant IEC 61010 laboratory electrical safety standards, IEC 61674 for medical electrical equipment, applicable GB/T standards for clinical laboratory equipment, and relevant medical device regulations (FDA, CE, NMPA). The instrument follows applicable electromagnetic compatibility standards. Reagents should be from qualified suppliers with traceable calibrators. Users should verify compliance with specific clinical laboratory accreditation requirements (ISO 15189, CAP, CLIA).
Q3: What is the warranty period for the whole machine and key components?
A: The whole auto chemistry analyzer is covered by a 12-month warranty. The sample handler, reagent system, optics, controller, software and housing are covered, while reagents, cuvettes, tubing and fuses are consumables. Damage from improper use or unauthorized repair is excluded. Extended service contracts are standard for this clinical diagnostic equipment.
Q4: Is this device difficult to operate? Is professional training required?
A: Operation requires trained clinical laboratory personnel familiar with chemistry analysis, quality control and regulatory requirements. We provide comprehensive training, operation manuals and application support. Proper sample handling, reagent setup, calibration, quality control, result review and biosafety procedures are critical for accurate results and regulatory compliance.
Q5: What is the typical lead-time for order delivery?
A: Standard models require 7-30 working days. In-stock units can ship within 3-7 working days. Custom configurations or large built-to-order systems may require additional time, and we confirm the exact schedule before order confirmation.
Q6: Is regular calibration required? What is the recommended calibration cycle?
A: Calibration with manufacturer calibrators per reagent lot or schedule. Quality control (normal and abnormal levels) per run or daily for clinical use. Optics and fluidics verified periodically. Software updates installed as needed. Full system performance verification annually. Routine maintenance of sample probe, reagent probe and mixing system per manufacturer schedule.
Q7: Are supporting consumables universal?
A: Reagents, calibrators, controls, cuvettes and tubing are typically manufacturer-specific, though some open-system analyzers accept third-party reagents. Long-term consumable cost depends on test volume and menu. Reagent compatibility should be verified for open systems.
Q8: Can I customize parameters or supporting accessories?
A: Customization includes test throughput, test menu, sample capacity, STAT capability, connectivity (LIS/HIS), barcode reading and accessories. Additional reagent kits and accessories can be ordered separately. Custom orders extend delivery lead-time.
Q9: Does the purchase include on-site installation and commissioning service?
A: Yes, auto chemistry analyzers include on-site installation, commissioning, calibration, validation and operator training by certified specialists. Site preparation guidance is provided before delivery to ensure power, water, drainage and IT requirements are met.
Q10: What types of samples are compatible with this equipment?
A: The auto chemistry analyzer analyzes serum, plasma, urine and other body fluids within the sample type, test menu and specification. Different tests require specific sample types (serum for most chemistry, plasma for some, urine for specific tests). Samples should be properly collected, centrifuged and free of hemolysis, lipemia or icterus that may interfere. Users should follow proper sample collection and handling protocols, use appropriate tubes and anticoagulants, calibrate per reagent lot, run quality controls per clinical laboratory standards, review results for flags and interferences, follow proper biosafety procedures for patient samples, and maintain proper documentation for regulatory compliance. The analyzer should be connected to LIS/HIS for result management. For critical results, proper notification procedures should be followed. The instrument should be maintained per manufacturer schedule, and probes should be cleaned regularly to prevent carryover. Waste should be disposed of per biological and chemical waste regulations. For clinical use, the laboratory should be accredited per applicable standards (ISO 15189, CAP, CLIA).
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