Characteristics
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Important Information
The PRECICHEK System is intended for in vitro
diagnostic use with capillary whole blood. The
system should not be used for diagnosis of diabetes
or for testing newborn infant (neonatal testing).
CAUTION
1. The user should not take any medical relevance
decision based on test result without first
consulting his or her medical practitioner.
2. Call your doctor immediately if you
experience symptoms that are not consistent
with your blood glucose test results.
3. Severe dehydration or excessive water loss
may cause false, high results. Call your doctor
right away if you suspect you are suffering
from dehydration.
4. For ACH Strip, A sample with large amount
of reducing substances such as triglycerides
(>1000mg/dL), ascorbic acid (>2.25mg/dL),
uric acid (>15mg/dL) and xylose (> 50mg/dL).
5. A red blood cell count (hematocrit) that is
either very high (over 55%) or very low (under
30%) can cause false result.
6. High altitudes above than 2,750 meter (8,800
feet) may affect the test results.
7. Temperatures outside the range of 10°C to 40°C
(50°F to 104°F) may affect the test results.
8. The meter and lancing device are for single
patient use. Do not share them with anyone
including other family members. Do not use
on multiple patients.
9. All parts of the kit are considered
biohazardous and can potentially transmit
infectious diseases, even after you have
performed cleaning and disinfection.
10. Do not use PRECICHEK system to test on
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