Introduction
A liquid based cytology processor is an instrument used for the preparation of the cytology specimens by the liquid based cytology (LBC) method, and it is used in the clinical, the pathology, the gynecology, and the many other applications. The liquid based cytology processor prepares the specimens by the collection of the cells in a liquid medium, the processing to remove the blood and the debris, and the preparation of a thin layer of the cells on a slide, which provides the improved and the consistent specimens for the cytological examination; the liquid based cytology processor consists of a sample processing system, a slide preparation system, the reagents and the filters, a control system, and the display, and it processes the multiple samples, with features such as the automated operation and the barcoding; the liquid based cytology processor is used for the preparation of the cervical cytology specimens, for the preparation of the specimens for the cytological diagnosis, for the screening, for the research, and for many other applications, and it is an essential instrument in the cytology laboratory. Liquid based cytology processors are used in the clinical laboratories, in the pathology, in the gynecology, in the research, and for many other applications. With their liquid based preparation, liquid based cytology processors are essential for the cytology specimen preparation.
Liquid-L2ased Cytology Processor T-LCP-S2101
Liquid-L2ased Cytology Processor T-LCP-S2102
Liquid-L2ased Cytology Processor T-LCP-S2100
Standards
ISO 20166-1:2018-Molecular in vitro diagnostic examinations-Specifications for pre-examination processes for FFPE tissue-Part 1: Isolated RNA
Complies with the above standards, but is not limited to them.
Features
1. Liquid-based cytology processor for preparing standardized cell samples from fluid specimens.
2. Automated cell collection, transfer and slide preparation for consistent cytology smears.
3. Suitable for gynecological cervical screening, non-gynecological cytology and clinical laboratories.
4. Reduces blood, mucus and inflammatory cell interference for improved specimen quality.
5. Includes processor, consumable kits, slides and operation software.
FAQ
Q1: What testing scenarios is this instrument mainly applied to?
A: The liquid-based cytology processor is used in clinical pathology laboratories, cytology screening centers, hospitals, cancer screening programs and research institutions to prepare standardized cell monolayers from liquid-based cytology specimens. It supports cervical cancer screening (Pap test), non-gynecological cytology including fine needle aspirations, body fluids, urine and respiratory specimens, and research cytology applications. The automated processing produces uniform, thin-layer cell preparations with reduced blood, mucus and inflammatory cell background, improving diagnostic accuracy and screening efficiency compared with conventional smears. It is essential for high-volume cytology laboratories and cancer screening programs requiring consistent, high-quality specimen preparation for reliable detection of abnormal cells, infectious agents and other cytological findings.
Q2: What standards does the instrument comply with?
A: The processor complies with IEC 61010 medical and laboratory electrical safety standards, relevant GB/T standards for medical laboratory equipment, and may reference ISO 15189 for medical laboratory quality. Cervical cytology screening follows applicable clinical guidelines including WHO and national cancer screening program protocols. Consumables should be used with compatible specimen collection systems.
Q3: What is the warranty period for the whole machine and key components?
A: The whole processor is covered by a 12-month warranty. The mechanism, controller and software are covered, while filters, tubing, processing kits and slides are consumables excluded from warranty. Damage from improper consumable use or unauthorized repair is excluded. Extended service contracts are available.
Q4: Is this device difficult to operate? Is professional training required?
A: Operation requires trained cytology laboratory personnel familiar with specimen handling and instrument operation. We provide structured training, operation manuals and application support. Proper specimen loading, consumable installation and daily maintenance are important for consistent slide quality.
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 maintenance required? What is the recommended maintenance cycle?
A: Daily cleaning of the processing chamber and fluid paths is recommended. Consumable replacement follows usage. Filter and tubing inspection monthly. Full preventive maintenance and calibration by a service engineer annually. Software updates follow the manufacturer schedule.
Q7: Are supporting consumables universal?
A: Processing kits, filters, slides and reagents are typically proprietary to the instrument system and should be sourced from the manufacturer or authorized distributor to ensure performance and warranty. Long-term consumable cost depends on specimen volume.
Q8: Can I customize parameters or supporting accessories?
A: Customization includes specimen capacity, processing protocol, slide type and software features. Additional consumable 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, cytology processors include on-site installation, commissioning and operator training by certified application specialists. Site preparation guidance is provided before delivery to ensure power, ventilation and space requirements are met.
Q10: What types of samples are compatible with this equipment?
A: The processor handles liquid-based cytology specimens including cervical samples, fine needle aspirations, body fluids, urine, respiratory and other cytology specimens collected in compatible preservative solutions. Specimens should be properly collected, labeled and transported according to clinical protocols. Users should follow the instrument operating instructions, use compatible consumables, perform quality control with known specimens, and ensure proper biosafety handling and waste disposal for clinical specimens.
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