Important Information: Read This First - i-SENS CareSens N Owner's Booklet

Important Information: Read This First!

For optimum safety and benefits, please read the entire manual
contents before using the system.
Intended use:
CareSens N NFC Blood Glucose Monitoring System is used for the
quantitative measurement of the glucose level in capillary whole
blood as an aid in monitoring diabetes management effectively at
home or in clinical settings.
CareSens N NFC Blood Glucose Monitoring System should be used
only for self-testing outside the body (in vitro diagnostic use only).
CareSens N NFC Blood Glucose Monitoring System should not
be used for the diagnosis of diabetes or for testing newborns.
Testing sites include the traditional fingertip testing along with
alternate site testing on forearm and palm.
Meaning of Symbols Used:
For in vitro diagnostic use
This product fulfills the requirements for Directive 98/79/
EC on in vitro diagnostic medical devices
Cautions for safety and optimum product use
Consult instructions for use
Do not discard this product with other household-type
waste
Use by (unopened or opened test strip vial)
Manufacturer
Do not reuse
Serial number
4 www.i-sens.com
Temperature limitation
Batch code
Authorised representative
• Glucose in blood samples reacts with the chemical in
the test strip to produce a small electrical current. The
CareSens N NFC meter detects this electrical current and
measures the amount of glucose in the blood sample.
• The CareSens N NFC Blood Glucose Meter is designed to
minimise code related errors in monitoring by using the
no-coding function.
• The CareSens N NFC Blood Glucose Meter should be used
only with the CareSens N Test Strips.
• An abnormally high or low red blood cell count (hematocrit
level over 65% or below 15%) may produce inaccurate
results.
• If your test result is below 60 mg/dL (3.3 mmol/L) or above
240 mg/dL (13.3 mmol/L), consult a healthcare professional
immediately.
• Inaccurate results may occur in severely hypotensive
individuals or patients in shock. Inaccurate low results
may occur for individuals experiencing a hyperglycemic-
hyperosmolar state, with or without ketosis. Critically ill
patients should not be tested with blood glucose meters.
• Inaccurate results may occur in patients undergoing
oxygen therapy.
If you need assistance, please contact your authorised i-SENS
sales representative or visit www.i-sens.com for more information.
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