iHealth BPM1AE Manuel du propriétaire - Page 7

Parcourez en ligne ou téléchargez le pdf Manuel du propriétaire pour {nom_de_la_catégorie} iHealth BPM1AE. iHealth BPM1AE 17 pages.

15.

Environmental temperature for storage and transport: -20

50 (-4 ～122 )

16.

Environmental humidity for storage and transport: ≤85%RH

17.

Environmental pressure: 80kPa-105kPa

18.

Battery life: more than 180 measurements on a full charge

19.

The blood pressure measurement system includes accessories, pump,

valve, cuff, and sensor.

Note: These specifications are subject to change without notice.

GENERAL SAFETY AND PRECAUTIONS

1. Read all of the information in the Owner's Manual and other provided

instructions before operating the unit.

2. Stay still, calm and rest for 5 minutes before blood pressure

measurement.

3. The cuff should be placed at the same level as your heart.

4. During measurement, neither speak nor move your body and arm.

5. Measuring on same arm for each measurement.

6. Please always relax at least 1 or 1.5 minutes between measurements

to allow the blood circulation in your arm to recover. Prolonged

over-inflation (cuff pressure exceed 300 mmHg or maintained above15

mmHg for longer than 3 minutes) of the bladder may cause ecchymoma

of your arm.

7. Consult your physician for any of the following situations:

a) The application of the cuff over a wound or inflamed area

b) The application of the cuff on any limb with intravascular access

or therapy, or an arterio-venous (A-V) shunt

c) The application of the cuff on the arm on the side of a mastectomy

d) Simultaneous use with other medical monitoring equipment on the

same limb

e) The blood circulation of the user needs to be checked

This Blood Pressure Monitor is designed for adults and should never

be used on infants, young children, pregnant or pre-eclamptic

patients. Consult your physician before use on children.

9. Do not use this product in a moving vehicle as this may result in

inaccurate measurements.

10.

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.

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