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NOTICE
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 cu 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 wrist 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 (cu pressure exceed 300 mmHg or maintained above15 mmHg for longer than 3
minutes) of the bladder may cause ecchymoma of your wrist.
7. Consult your physician if you have any doubt about below cases:
1) The application of the cu over a wound or inflammation diseases;
2) The application of the cu on any limb where intravascular access or therapy, or an arterio-venous (A-V) shunt, is
present;
3) The application of the cu 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 Sphygmomanometers is designed for adults and should never be used on infants or young children.
Consult your physician or other health care professionals 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 cu/stethoscope auscultation method, within the limits prescribed by the American National Standard
Institute, Electronic or automated sphygmomanometers.
11. 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 part ELECTROMAGNETIC
COMPATIBILITY
INFORMATION.
12. If Irregular Heartbeat (IHB) brought by common arrhythmias is detected in the procedure of blood pressure
measurement, a signal of will be displayed. Under this condition, the Electronic Sphygmomanometers can keep
function, but the results may not be accurate, it’s suggested that you consult with your physician for accurate
assessment.
There are 2 conditions under which the signal of IHB will be displayed:
1) The coecient of variation (CV) of pulse period >25%.
2) The dierence of adjacent pulse period≥0.14s, and the number of such pulse takes more than 53 percentage of the
total number of pulse.
13. Please do not use the cu other than supplied by the manufacturer, otherwise it may bring biocompatible hazard and
might result in measurement error.
14. The monitor might not meet its performance specifications or cause safety hazard if stored or used outside the
specified temperature and humidity ranges in specifications.
15. Please do not share the cu with other infective person to avoid cross-infection.
16. This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part
15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a
residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to radio communications. However,
there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful
interference to radio or television reception, which can be determined by turning the equipment o and on, the user is
encouraged to try to correct the interference by one or more of the following measures:
— Reorient or relocate the receiving antenna.
5


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