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9. While the given device is able to detect specic pulse arrhythmia, the measurement
accuracy of the blood pressure meter may be impaired with the occurrence of pulse
arrhythmia.
10. To stop operation at any time, press the ON/OFF/START key, and the air in the cu will
be rapidly exhausted.
11. Once the ination reaches 300 mmHg, the unit will start deating rapidly for safety
reasons.
12. Please note that this unit can be a home healthcare product, but it is not intended to
serve as a substitute for the advice of a physician or medical professional.
13. Do not use this device for diagnosis or treatment of any health problem or disease.
Measurement results are for reference only. Consult a healthcare professional for in-
terpretation of pressure measurements. Contact your physician if you have or suspect
any medical problem. Do not change your medications without the advice of your
physician or healthcare professional.
14. Electromagnetic interference: The device contains sensitive electronic components.
Avoid strong electrical or electromagnetic elds in the direct vicinity of the device (e.g.
mobile telephones, microwave ovens). These may lead to temporary impairment of
measurement accuracy.
15. Dispose of device, batteries, components and accessories according to local regula-
tions.
16. This monitor may not meet its performance specication if stored or used outside
temperature and humidity ranges specied in Specications.
17. Please note that when inating, the functions of the limb in question may be impaired.
18. During the blood pressure measurement, blood circulation must not be stopped for
an unnecessarily long time. If the device malfunctions, remove the cu from the arm.
19. Avoid any mechanical restriction, compression or bending of the cu line.
20. Do not allow sustained pressure in the cu or frequent measurements. The resulting
restriction of the blood ow may cause injury.
21. Ensure that the cu is not placed on an arm in which the arteries or veins are undergo-
ing medical treatment, e.g. intravascular access or therapy, or an arteriovenous (AV)
shunt.
22. Do not apply the cu on the side, where a mastectomy has been performed in your
patient history.
23. Do not place the cu over wounds as this may cause further injury.
24. Only ever use the cus provided with the monitor or original replacement cus. Oth-
erwise erroneous results will be recorded.
25. Batteries can be fatal if swallowed. You should therefore store the batteries and prod-
ucts where they are inaccessible to small children. If a battery has been swallowed, call
a doctor immediately.
26. Do not use the tubing and/or AC adaptor for any other purpose than those specied,
as they can cause risk of strangulation.
27. Do not service or maintain device and cu while in use.
Specications
Measurement Method Oscillometric
Measurement Range Pressure: 30~260 mmHg; Pulse: 40~199 beats/
minutev
Pressure Sensor Semi conductor
Accuracy Pressure: ± 3 mmHg; Pulse: ± 5% of reading
Inflation Pump Driven
Deflation Automatic Air Release Valve
Memory capacity 90 memories
Auto-shut-off 1 minute after last key operation
Permissible Operating
Temperature and Humidity
10°C~40°C (50°F~104°F); 15%~85% RH; 700~1060
hPa
Permissible Transport and Storage
Temperature and Humidity
-10°C~60°C (14°F~140°F); 10%~90% RH; 700~1060
hPa
DC Power Source DC 6V four AA Batteries
AC Power Source DC 6V, ≥600mA (Plug size: outer(-) is Ø4.0, inner(+)
is Ø1.7)
Dimensions 173.0 (L) X 115.0 (W) X 64.5 (H) mm
Weight 410g (G.W.) (w/o Batteries)
Arm circumference L: 34~46 cm (13.4”~18.1”); M: 24~36 cm
(9.4”~14.2”); S: 16~26 cm (6.3”~10.2”)
Limited Users Adult users
:
Type BF: Device and cuff are designed to provide
special protection against electrical shocks.
IP Classification IP21: Protection against harmful ingress of water
and particulate matter
* Specifications are subject to change without notice.
Electromagnetic Compatibility Information
1. This device needs to be installed and put into service in accordance with the
information provided in the user manual.
2. WARNING: Portable RF communications equipment (including peripherals such
as antenna cables and external antennas) should be used no closer than 30 cm
(12 inches) to any part of the X9, including cables specied by the manufacturer.
Otherwise, degradation of the performance of this device could result.
If higher IMMUNITY TEST LEVELS than those specied in Table 9 are used, the minimum
separation distance may be lowered. Lower minimum separation distances shall be
calculated using the equation specied in 8.10.
Manufacturer’s declaration-electromagnetic immunity
The X9 is intended for use in the electromagnetic environment specied below. The customer or the user of the X9 should assure that
is used in such and environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment-guidance
… 9

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