Function and Application:
For the identification of bacteria and fungi, as well as antimicrobial susceptibility testing, in various clinical infectious specimens.
★Detection Principle:
Microbial Identification (ID): Colorimetry and Turbidimetry to analyze bacterial physiological and biochemical reactions
Antibiotic susceptibility test (AST): Broth dilution testing to get minimum inhibitory concentration (MIC) of antibiotics.
Photoelectric detection per well, utilizing fiber optic light source transmission technology, ensuring no cross-interference between wells and eliminating the need for manual verification.
Bacterial Identification:
Capable of identifying over 500 microorganisms, including Enterobacteriaceae, non-fermenters, Staphylococcus, Enterococcus, Streptococcus, Moraxella catarrhalis, Vibrio, and fungi, meeting clinical requirements.
Bacterial AST:
Performs susceptibility testing for Enterobacteriaceae, non-fermenters, Vibrio, Staphylococcus, Streptococcus, Enterococcus, and Haemophilus. Capable of detecting and reporting resistance phenotypes or mechanisms such as ESBL, MRSA, VRE, Carbapenem resistance, Erythromycin-induced Clindamycin resistance (D-test), High-level Gentamicin resistance, and High-level Streptomycin resistance.
Fungal AST:
Includes antifungal agents such as Caspofungin, Micafungin, Amphotericin B, 5-Flucytosine, Voriconazole, Fluconazole, and Itraconazole.
★Throughput:
Capable of incubating 64 reagent cards simultaneously.
★Turnaround Time:
4–24 hours; ≤6 hours for common bacteria.
★Automation:
Features automatic barcode reading of reagent cards, automatic incubation, detection, interpretation, disposal of waste cards, automatic analysis and transmission of results to the Laboratory Information System (LIS), and automatic result printing.
★No Auxiliary Reagents Required:
Operation does not require the addition of supplementary reagents.
Standardization:
Uses an electronic Nephelometer for standardized preparation of bacterial suspensions and an Automated Liquid Handling System for standardized, automated sample loading.
Software & Interface:
Features muti-language operating software and provides interfaces for LIS or Hospital Information System (HIS).
Expert System:
Equipped with an open expert system that adheres to CLSI, EUCAST, and other standards to provide suggestions and modifications.
Epidemiological Statistics:
Generates statistical analysis reports including bacterial distribution, detection rates, susceptibility rates, and departmental workload. Data can be exported to Excel for further processing.
Data Export & Reporting:
Supports data export compatible with WHONET software for statistical analysis and allows uploading to the CARSS (China Antimicrobial Resistance Surveillance System) network for resistance data reporting.
Hospital Infection Control Module:
Allows input of hospital infection microbial culture reports (e.g., hand hygiene, air cultures, surface swabs). Users can configure whether these reports are transmitted to the LIS.
Reports drug S/I/R (Susceptible/Intermediate/Resistant) results and MIC values grouped by categories A, B, C, O, U, and I in accordance with CLSI standards. Allows flexible selection of grouping or hierarchical reporting formats.
★CDC Customization:
Features antimicrobial susceptibility panels customized for the China CDC system and provides documentation for the 2024 version of the CDC customization scheme. 2.17 Customer Customization: Offers customer-customized AST panels with antibiotic combinations tailored to client needs for research and other purposes. 3. Detection Reagents
★Panel Types:
Provides combined ID and AST panels; also available are standalone AST panels. (XK-96A-C. XK-96A-F, XK-96A-P, XK-96A-L, XK-96A-Z; XK-96B-C, XK-96B-F, XK-96B-P, XK-96B-L)
Reading Modes:
Supports both automatic instrument reading and manual interpretation for flexible result reporting.
★Biosafety Design:
The 96-well detection panels are equipped with dedicated panel covers. Covering the panel after inoculation ensures laboratory biosafety and sample security.
Quality System:
Holds the Medical Device Registration Certificate of the People's Republic of China, ISO 9001 Quality Management System Certification, and ISO 13485 Medical Devices Quality Management System Certification.
Note: Parameters marked with "★" denote key technical specifications.
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