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Product Details:
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| Brand Name:: | Poweray | Transport Package:: | Box/Carton |
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| Display Of Result: | HbA1C:NGSP+IFCC/CRP:CRP+hsCRP | Product Name:: | Specific Proteins Analyzer |
| Weight: | 3KGS | Application: | Rapid Test Kit |
| Test Result: | Quantitative | ||
| High Light: | Hemoglobin A1C Specific Protein Analyzer,3 Channel Biochemistry Hba1c Analyser,3 Channel Hemoglobin A1C Analyser |
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Introduction
POCT immunoassay analyzer is used for in vitro detection of human serum/plasma/ whole blood/urine samples in hospital, assisting clinical diagnosis of myocardial infarction, myocardial injury, heart failure, acute coronary syndrome, cardiovascular inflammation, venous thromboembolism, inflammation, bacterial/viral infection identification, neonatal sepsis, acute and chronic kidney disease, also routine early detection and early treatment of kidney injury, diabetes and other diseases.
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
