15
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 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-ination
(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 if you have any doubt about below cases:
•The application of the cuff over a wound or inammation diseases; •The application of the cuff on any
limb where intravascular access or therapy, or an arterio-venous (A-V) shunt, is present; •The application
of the cuff on the arm on the side of a mastectomy; •Simultaneously used with other monitoring medical
equipments on the same limb; •Need to check the blood circulation of the user. 8. This Electronic Sphyg-
momanometers 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 cuff/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 coefcient of variation (CV) of pulse
period >25%. 2) The difference 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 cuff 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 specications or cause safety hazard if stored or used outside the
specied temperature and humidity ranges in specications. 15. Please do not share the cuff with other
infective person to avoid cross-infection. 16. Medical AC adapter which output is DC 6.0V 600mA and
complied with IEC 60601-1/EN 60601-1/UL 60601-1 and IEC 60601-1-2/EN 60601-1-2/UL 60601-1-2 is
suitable for this monitor. Please note that the monitor jack size: hole O5.5mm, center pin O2.0mm. Please
pay attention to polarity. 17. 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 off 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. •Increase the separation between the equipment and receiver. •Connect the equipment into an
outlet on a circuit different from that to which the receiver is connected. •Consult the dealer or an expe-
rienced radio/TV technician for help. 18. This blood pressure monitor is veried by auscultatory method. It
is recommended that you check annex B of ANSI/AAMI SP-10 :2002 + A1 : 2003 + A2 : 2006 for details of
verication method if you need.
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