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Limitations of the measurement procedure
1. DO NOT use serum or plasma sample.
2. DO NOT use neonate blood sample.
3. Extreme humidity may affect the results. A relative humidity
greater than 90% may cause incorrect results.
4. The System is designed to be used at temperatures between
10°C and 40°C (50°F and 104°F). Outside this range, the sys-
tem may yield erroneous results.
5. DO NOT reuse the test strips. The test strips are intended for
single use only.
6. DO NOT use iodoacetic acid, uoride or sodium uoride/oxalate
as a preservative for blood specimens.
7. Hematocrit:
Test strip results are not signicantly affected by hematocrits
in range of 30% to 55%. Hematocrit levels less than 30% may
cause incorrect high readings and hematocrit levels greater
than 55% may cause incorrect low readings. If you do not know
your hematocrit level, consult your healthcare professional.
8. Interfering substances depend on the concentration. The sub-
stances below may affect the test results:
• Acetaminophen > 15 mg/dL or 1.0 mmol/L
• Geneticist Acid > 8 mg/dL or 0.5 mmol/L
• Levodopa > 10 mg/dL or 0.5 mmol/L
• Dopamine > 13 mg/dL or 0.7 mmol/L
• Methyldopa > 2.5 mg/dL or 0.12 mmoll/L
• Uric Acid >14 mg/dL or 0.4 mmol/L
86


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