c. If an Irregular Heartbeat (IHB) is detected during a measurement, the IHB
symbol will be displayed (blinking). If an IHB is detected, the results of
the blood pressure measurement may be inaccurate. Please consult your
healthcare provider for an accurate assessment.
d. Your results will appear on the tablet screen. Press yes to accept, your
results will now be added and trended.
e. The monitor will automatically switch off after one minute to save the
batteries. Alternatively, you can press the “START/STOP” button to turn
off the monitor manually.
f. At any time during a measurement, you can interrupt a measurement
by pressing the“START/STOP” button.
CLASSIFICATION OF BLOOD PRESSURE
BLOOD PRESSURE SYSTOLIC mm Hg DIASTOLIC mm Hg
CATEGORY (upper number) (upper number)
NORMAL LESS THAN 120 and LESS THAN 80
ELEVATED 120–129 and LESS THAN 80
HIGH BLOOD PRESSURE
(HYPERTENTION) STAGE 1 130–139 or 80 - 89
HIGH BLOOD PRESSURE
(HYPERTENTION) STAGE 2 140 OR HIGHER or 90 OR HIGHER
HYPERTENSIVE CRISIS
(consult your doctor HIGHER THAN 180 and/or HIGHER THAN 120
immedediately)
6. TROUBLESHOOTING SECTION
PROBLEM POSSIBLE CAUSE SOLUTION
LCD shows low
battery icon
LCD shows “Er 0”
LCD shows “Er 1”
LCD shows “Er 2”
LCD shows “Er 3”
LCD shows “Er 4”
LCD shows “Er 5”
LCD shows “Er 6”
LCD shows “Er 7”
LCD shows “Er 8”
LCD shows “Er 9”
No response when you
press button or load
battery
7. GENERAL SAFETY AND PRECAUTIONS
1. Carefully read the user guide before operating the device.
2. 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 the arm on the side of a mastectomy.
c) Simultaneous use with other medical monitoring equipment on the
same limb.
d) The application of the cuff on any limb with intravascular access or
therapy, or an arteriovenous (A-V ) shunt.
e) The blood circulation of the user needs to be checked.
3. Do not use this product in a moving vehicle as this may result in
inaccurate measurements.
4. The IHB symbol will be displayed under 2 sets of circumstances:
a) The coefficient of variation (CV ) of pulse period >25%.
b) The difference of adjacent pulse period is ≥0.14s and more than 53%
of the total number of pulse readings falls within this definition.
5. Please do not use any cuff other than that supplied as this may result in
inaccurate measurements.
6. The monitor will show 'HI' or 'Lo' as technical alarm on LCD if the
determined blood pressure (systolic or diastolic) is outside the rated
range specified in part SPECIFICATIONS. In this case, you should consult
a physician or check if you followed the operating instructions. The
technical alarm condition (outside the rated range) is pre-set in the
factory and cannot be adjusted or inactivated. This alarm condition is
assigned as low priority according to IEC 60601-1-8. The technical alarm
is non-latching and needs no reset. The signal displayed on LCD will
disappear automatically after about 8 seconds.
This Monitor is designed for adults and should never be used on
infants, young children or patients with preeclampsia.
This product might not meet its performance specifications if stored
or used outside the specified temperature and humidity ranges.
Please do not share the cuff with any infectious person to avoid
cross-infection.
7. Prolonged over-inflation of the cuff may cause bruises on your arm.
8. CARE AND MAINTENANCE
1. Do not drop the monitor or subject it to strong impacts.
2. Avoid high temperature and direct exposure to the sun. Do not immerse
the monitor in water.
3. If this monitor is stored near freezing temperatures, allow it to acclimate
to room temperature before use.
4. Do not attempt to disassemble this monitor.
5. If you do not use the monitor for a long time, please remove the
batteries.
6. It is recommended that the performance of this monitor be checked
every 2 years.
7. Please clean the monitor with a soft dry cloth. Do not use any abrasive or
volatile cleaners.
8. It is recommended that if the cuff is used in a hospital or a clinic, it be
disinfected twice a week. Wipe the inner side (the side that contacts skin)
of the cuff with a soft cloth lightly moistened with Ethyl alcohol (75-90%).
Then air dry the cuff.
10. The monitor can maintain the safety and performance characteristics for
a minimum of 10,000 measurements or three years, and the cuff integrity
is maintained after 1,000 open-close cycles of the closure.
9. WARRANTY
This device has been developed and validated by the manufacturer with a
team of medical specialists and engineers to be user friendly and clinically
accurate. It has been validated against the ESH Standard (European Society of
Hypertension) and can be used in a home, medical or clinical
environment. The device carries a two-year warranty.
If you have any questions regarding the aftersales or usage of the product,
please contact the distributor.
Low Battery
Pressure system is unstable
before measurement
Failed to detect systolic pressure
Failed to detect diastolic pressure
Pneumatic system is blocked
or the cuff is too tight during
inflation
Pneumatic system leakage or
the cuff is too loose during
inflation
Cuff pressure is above
300mmHg
More than 3 minutes with the
cuff pressure above 15 mmHg
EEPROM accessing error
Device parameter checking error
Pressure sensor parameter error
Incorrect operation or strong
electromagnetic interference
Change the batteries.
Don’t move and try again.
Apply the cuff correctly and
try again.
Measure again after five minutes.
If the monitor is still abnormal,
please contact the distributor.
Remove batteries, wait 5 minutes
then reinstall.
