Lifotronic Immunofluorescence Analyzer FA 160 with Incubation Function
- Category: >>>
- Supplier: Guangzhou Labon Medical Equipment Co. Limited
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Product Overview
Description
Products Description
Advanced Technology Automatic Fluorescence Immunoassay Analyzer FA-160 For Medical Diagnosis
Product Introduction:
FA-160 is testing platform with 12 testing channels and continuous sample introduction, based on fluorescence immunochromatographic technology. It covers the diagnosis of infection, cardiovascular diseases and diabetes,supporting whole blood, serum and plasma sample testing and making accurate and quantitative reports available in 3-15 minutes.
Test Menu:
1. Infection: hsCRP+CRP, PCT
2. Cardiac Markers: NT-proBNP, CK-MB, cTnI, Myo, 2 In 1(CK-MB/cTnI), 3 In 1(CK-MB/cTnI/Myo)
3. Diabetes: HbA1c
4. Coagulation: D-Dimer
2. Cardiac Markers: NT-proBNP, CK-MB, cTnI, Myo, 2 In 1(CK-MB/cTnI), 3 In 1(CK-MB/cTnI/Myo)
3. Diabetes: HbA1c
4. Coagulation: D-Dimer
Advantages of our FA-160 Testing Platform
1. Support 12 multiple tests at the same time
2. Twelve testing channels, with an actual velocity measurement of 120T
3. Scan and identify the testing items as well as the reagent strips come out automatically after the finished testing.
4. Multiple testing items, make medical examination efficient and rapid.
5. The data can be uploaded to LIS and printed automatically
2. Twelve testing channels, with an actual velocity measurement of 120T
3. Scan and identify the testing items as well as the reagent strips come out automatically after the finished testing.
4. Multiple testing items, make medical examination efficient and rapid.
5. The data can be uploaded to LIS and printed automatically
Performance specification
Accuracy: In this analyzer, the relative deviation of the measurement results in tests should be less than or equal to ±15%.
Stability: Turn on an analyzer that can work at stable working status, then use it to test result at the initial stage. Compared
the initial result with those tested 4hour and 8hour later, the relative bias should be no more than ±10%.
Repeatability: CV≤10%
Linear correlation coefficient: r≥0.9700
Stability: Turn on an analyzer that can work at stable working status, then use it to test result at the initial stage. Compared
the initial result with those tested 4hour and 8hour later, the relative bias should be no more than ±10%.
Repeatability: CV≤10%
Linear correlation coefficient: r≥0.9700
Information Details
technical parameters | ||||||||
Detection method | Immunofluorescence quantitative chromatography | |||||||
Power supply | A.C.100V—240V，50/60Hz/ Lithium battery: 7.4V | |||||||
External connection method | network cable, USB cable (less than 3 meters) | |||||||
External communication method | USB | |||||||
Optical performance | Excitation spectrum: 365nm Receiving spectrum: Central wavelength 613nm | |||||||
Storage capacity | 500000 patient records | |||||||
Display mode | 7 inch touch screen | |||||||
Indicator status | Running indicator: Green (This indicator turns green in the process of testing ) Power indicator: Green | |||||||
Environment conditions | Temperature：10℃~30℃ Relative humidity：≤70% Altitude: not more than 2000 meters Indoor / outdoor use: For indoor use only. Power voltage fluctuation should not exceed ± 10% of nominal voltage. Transient overvoltage category (overvoltage category) Ⅱclass Pollution level: 2 level | |||||||
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