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Product Details:
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Type: | Immunoassay System, Biochemistry Analyzer | Place Of Origin: | Shenzhen Guangdong |
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Warranty: | 1 Year | Transport Package:: | Box/Carton |
Display Of Result: HbA1C:: | NGSP+IFCC/CRP:CRP+hsCRP | Display:: | Colored HD Touchscreen |
High Light: | Hba1c Crp Biochemistry Analyzer,CE Approved Portable Biochemistry Analyzer,Biochemistry Analyser For Hba1c Crp |
1.Measuring method: Boric acid affinity chromatography
2.Sample type: whole blood
3.Immediate testing: the samples are inspected as soon as they arrive.
4.Smart and efficient: It only takes 2 minutes and a half from sample addition to test completion.
5.Easy to operate: The calibration curve comes with the reagent calibration card, no need to make a standard curve by yourself.
Comes with a timer: the instrument can start a timer at the same time, without additional configuration timer to complete the test.
Automatic measurement: Close the measurement handle to start the test automatically without the need to manually click the button.
6.Display: 3.5 inch color LCD touch display, small and convenient
7.Device expansion: support data transmission to LIS and HIS system, support external Bluetooth printer
Application Department
Widely used in social health, outpatient, emergency departments of various hospitals, ICU, laboratory, endocrinology and other departments.
Technical Specifications:
1. Results reporting unit Glycated hemoglobin (HbA1c) is reported in IFCC (mmol/mol) and derived NGSP units (%).
2. Accuracy:The reference substance is used as a sample for testing, and the relative deviation of the measurement results of
the analyzer should be within ±8%.
3. Repeatability: For samples with a concentration of 4.0%-6.5% (20.2mmol/mol-47.5mmol/mol), the coefficient of variation CV of
the repeated measurement results of the analyzer should not be greater than 3.0%.
4. Linear: In the detection range of the analyzer [4%-14%], the linear correlation coefficient r of the detection result should
not be less than 0.9900.
5. Stability:Within 8 hours after the start-up is stable, the relative deviation of the results of testing the same normal
sample should not exceed ±3.0%.
Contact Person: Ms. Carina
Fax: 86-755-89366646