iHealth View BP7S Mode D'emploi page 10

3. Do not use this product in a moving vehicle as this may result in inaccurate measurements.
4. Blood pressure measurements determined by this product are equivalent to those obtained by professional
healthcare practitioners using the cuff/stethoscope auscultation method within the limits prescribed by the
American National Standard, Electronic or Automated Sphygmomanometer. This device is also clinically
validated according to the 2010 Protocol of the European Society of Hypertension (ESH 2010).
5. If an Irregular Heartbeat (IHB) is detected during the measurement procedure, the IHB symbol will be
displayed in the "iHealth MyVitals" APP. Under this condition, the Wireless Blood Pressure Wrist Monitor can
keep functioning, but the results may be inaccurate. Please consult your physician for accurate assessment.
The IHB symbol will be displayed under 2 conditions:
1) The coefficient of variation (CV) of pulse period >25%.
2) The difference of adjacent pulse period is ≥0.14s and more than 53 percent of the total number of pulses
readings falls within this definition.
6. Please do not use any cuff other than that supplied by the manufacturer as this may result in inaccurate
measurements.
7. For information regarding potential electromagnetic or other interference between the blood pressure monitor
and other devices together with advice regarding avoidance of such interference, please see ELECTROMAG-
NETIC COMPATIBILITY INFORMATION. It is suggested that the blood pressure monitor should be operated at
least 10 meters away from electric or wireless devices (e.g. routers, microwave oven, etc.)
8. If the blood pressure measurement (systolic or diastolic) is outside the rated range specified in part
SPECIFICATIONS, the monitor will immediately display a technical alarm on the screen. In this case, repeat
the measurement ensuring that the proper measurement procedures are followed and/or consult with your
medical professional. The technical alarm is preset in the factory and cannot be adjusted or inactivated. This
technical alarm is assigned as low priority according to IEC 60601-1-8. The technical alarm does not need to
be reset.
9. This device requires a medical AC adapter with an output of DC 5.0V that complies with IEC 60601-1/UL
60601-1 and IEC 60601-1-2/EN 60601-1-2 such as ASP5-05010002JU (input: 100-240V, 50/60Hz, 200mA;
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