AEG BMG 5611 Mode D'emploi page 84

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12. Environmental temperature for operation: +10 °C to +40 °C (50 °F to 104 °F)
13. Environmental humidity for operation: ≤ 90 % RH
14. Environmental temperature for storage and transport: -20 ° to 55 °C (-4 ° to 131 °F)
15. Environmental humidity for storage and transport: ≤ 90 % RH
16. Environmental pressure: 80 kPa to 105 kPa
17. Battery life: Approx 500 measurements
18. A list of all components belonging to the pressure measuring system, including acces-
sories: Pump, valve, LCD, cuff, sensor
Note:
These specifications are subject to change without notice.
NOTICES
1. Read all of the information in the operation guide and any other literature in the box
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 each time.
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 mm Hg or maintained above 15 mm Hg for longer than 3 minutes) of the bladder
may cause ecchymoma of your arm.
7. Consult your physician if you have any doubt about below cases:
1) The application of the cuff over a wound or inflammation diseases;
2) The application of the cuff on any limb where intravascular access or therapy, or an
arterio-venous (A-V) shunt, is present;
3) The application of the cuff on the arm on the side of a mastectomy;
4) Simultaneously used with other monitoring medical equipments on the same limb;
5) Need to check the blood circulation of the user.
8.
This Electronic Sphygmomanometer is designed for adults and should never be
used for infants or young children. Consult your physician or other health care profes-
sionals before use on older children.
9. Do not use this unit in a moving vehicle, This may result in erroneous measurement.
10. Blood pressure measurements determined by this monitor are equivalent to those
obtained by a trained observer using the cuff/stethoscope auscultation method, within
the limits prescribed by the American National Standard Institute, Electronic or auto-
mated sphygmomanometers.

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