EN
tout Kategori
EN

Seri Siveyans glikoz nan san

San danje AQ Smart

Fast 5s test time; FDA-GDH monitoring system; SINODRAW patent lancing device; Temperature warning

apèsi sou lekòl la
  • apèsi sou lekòl la

    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.

  • Prensip egzamen an

    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.

  • Karakteristik (avantaj teknik)

    1) FAD-GDH system : It is not easily affected by oxygen molecule in the blood.

    2) User-friendly operation system: no coding & automatic test strip ejectionin the management of diabetes.

Spesifikasyon
Volim san 0.6μL
Kalite Egzanp Antye san antye kapilèr ​​san
Kalibrasyon Plasma ekivalan
Mezire tan 5s
Meter depo / kondisyon transpò -20~ 55 ℃
dimansyon 84 * 60 * 26 (mm)
pwa 73.5g, with battery
Sous pouvwa 3V DC, 50mA, 2 pil AAA asid
Memwa 10 rezilta tès glikoz nan san
Kondisyon fonksyònman KOUMAN POU ~ 10; ≤80% RH
konstriksyon divizyon Men ki te kenbe
Inite mezi yo mg / dL oswa mmol / L
Ranje Mezi 20~600 mg/dL or 1.1~33.3mmo/L
etajè lavi 10 ane (estime pa 7 tès fwa pou chak jou).
Pandan itilizasyon, itilizatè ta dwe kenbe pwodwi an
gade kondisyon manyèl sa a.
Karakteristik Pèfòmans

Accuracy: 95% test result of Safe AQ meet the requirement below:

Concentration Range Bias%
<5.5 mmol/L(100 mg/dL) Within±0.83 mmol/L(15 mg/dL)
25.5 mmol/L(100mg/dL) Nan ± 15%

Precision: test result of Safe AQ Smart meet the requirement below:

Concentration Range Require ment
<5.5 mmol/L(100 mg/dL) SD<0.34mmol/L(6.0mg/dL)
25.5 mmol/L(100mg/dL) CV<6.0%