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Safe AQ Smart
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Sinodraw Patent Lancing Device
Têgihiştinî
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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.
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Prensîba testê
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.
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Taybetmendî (avantajên teknîkî)
1) Pergala FAD-GDH: Ji hêla molekula oksîjenê ve di xwînê de bi hêsanî bandor nabe.
2) Pergala xebitandina heval-heval: ne kodkirin & nexşeya testa otomatîk ejectionin rêveberiya şekirê.
Specification
| Hejmara xwînê | 0.6μL |
| Cûreyê nimûneyê | Capillary xwîna tevahî xwînê |
| Vebijêrk | Hevkêşeya plazmayê |
| Mezinahiya demê | 5s |
| Rewşa depokirin / veguhastina metreyê | -20℃~ 55 |
| Ebat | 84 * 60 * 26 （mm |
| Pîvan | 73.5g, with battery |
| Çavkaniya hêza | 3V bataryayên alkalîn ên DC, 50mA, 2 |
| Bîr | 10 encamên testa glukoza xwînê |
| Rewşa xebitandinê | 10 ℃ ~ 35℃; ≤80% RH |
| avahî | Hand-girtin |
| Yekîneyên pîvandinê | mg / dL an mmol / L |
| Rêzeya pîvanê | 20 ~ 600 mg / dL an 1.1 33.3 mmo / L |
| Jiyanê Shelf | 10 sal (bi ceribandinê rojê 7 caran tê texmîn kirin.) Di dema karanînê de, pêdivî ye ku bikarhêner hilberê bidomîne hewcedariyên vê manualê bikarhêner bişînin. |
Taybetmendiyên performansî
Accuracy: 95% test result of Safe AQ meet the requirement below:
| Range Concentration | Bias% |
|---|---|
| <5.5 mmol / L (100 mg / dL) | Di nav ± 0.83 mmol / L (15 mg / dL) |
| 25.5 mmol / L (100mg / dL) | Di nav ± 15% |
Precision: test result of Safe AQ Smart meet the requirement below:
| Range Concentration | Pêdivî ye |
|---|---|
| <5.5 mmol / L (100 mg / dL) | SD <0.34mmol / L (6.0mg / dL) |
| 25.5 mmol / L (100mg / dL) | CV <6.0% |
