EN 
ES
PT
TH
DE
TR
FR
Safe AQ Smart
Fast 5s test time; FDA-GDH monitoring system; SINODRAW patent lancing device; Temperature warning
Têgihiştinî
Têgihiştinî
The Safe AQ Smart Blood Glucose Monitoring System is designed for the quantitative measurement of glucose in fresh capillary whole blood samples taken from the fingertip and in venous whole blood samples. The Blood Glucose Monitoring System is for use outside the body only (in vitro diagnostic use) for self-testing and professional use as an aid in the management of diabetes.
Test principle
A blood glucose test is based on measurement of electrical current caused by the reaction of glucose with the reagents (special chemicals) on the electrode of the strip. The blood or control solution sample is drawn into the tip of the test strip through capillary action. Glucose in the sample reacts with the special chemicals and generates electrons, which produce electrical current. The blood glucose meter measures the electrical current and calculates the glucose result. The glucose result is displayed by your meter as mg/dL or mmol/L.
Taybetmendî (Tiştên teknîkî)
1) Pergala FAD-GDH: Ew bi hêsanî bi molekulên oksîjenê di xwînê de bandor nabe.
2) Pergala xebitandinê ya bikarhêner-heval: Naha kodkirina & ceribandina otomatîk ejectionin di rêveberiya diyabetê de.
Specification
| Bêjeya xwînê | 0.6μL |
| Cureyê nimûneyê | Bi tevahî xwîna capillary xwînmij |
| Vebijêrk | Plasma wekhev |
| Mezinahiya demê | 5s |
| Rewşa hilanînê / veguheztina metroyê | -20℃~ 55 |
| Ebat | 84 * 60 * 26 （mm |
| Pîvan | 73.5g, with battery |
| Çavkaniya hêza | 3V DC, 50mA, 2 AAA alkaline batteries |
| Bîr | Encamên testa glîkozê ya xwînê 10 |
| Ertê xebatê | 10 ~ 35℃; ≤80% RH |
| avahî | Hand-girtin |
| Yekîneyên pîvanê | mg / dL an mmol / L |
| Rêzeya pîvanê | 20 ~ 600 mg / dL an 1.1 ～ 33.3mmo / L |
| Jiyanê Shelf | Salên 10 (ji hêla ceribandina 7 car per roj estimated ve hat texmîn kirin). Di dema karanîna, divê bikarhêner hilberê bigirin li gorî pêdiviyên manuala vê bikarhênerê binihêrin. |
Taybetmendiyên performansî
Accuracy: 95% test result of Safe AQ meet the requirement below:
| Rêza Concentration | Bias% |
|---|---|
| <5.5 mmol / L (100 mg / dL) | Bi 0.83 15 mmol / L (XNUMX mg / dL) |
| 25.5 mmol / L (100mg / dL) | Bi ± 15% |
Precision: test result of Safe AQ Smart meet the requirement below:
| Rêza Concentration | Requ ment |
|---|---|
| <5.5 mmol / L (100 mg / dL) | SD <0.34 mmol / L (6.0mg / dL) |
| 25.5 mmol / L (100mg / dL) | CV <6.0% |
