PULOX PO-200A Mode D'emploi page 18

explosive materials, high temperature and moisture.
 If the oximeter gets wet, please stop operating it.
 When it is carried from cold environment to warm or humid
environment, please do not use it immediately.
 DO NOT operate keys on front panel with sharp materials.
 High temperature or high pressure steam disinfection of the
oximeter is not permitted. Refer to User Manual in the relative
chapter for instructions of cleaning and disinfection.
 Do not have the oximeter immerged in liquid. When it needs
cleaning, please wipe its surface with medical alcohol on soft
tissue. Do not spray any liquid on the device directly.
 When cleaning the device with water, the temperature should be
lower than 60°C.
 As to the fingers which are too thin or too cold, it would probably
affect the normal measure of the patients' SpO2 and pulse rate,
please clip a thicker finger such as thumb and middle finger deeply
enough into the probe.
 Do not use the device on infant or neonatal patients.
 The product is suitable for children above four years old and adults
(weight should be between 15kg and 110kg).
 The device may not work for all patients. If you are unable to
achieve stable readings, discontinue use.
 The update period of data is less than 5 seconds, which is
changeable according to different individual pulse rate.
 The waveform is normalized. Please read the measured value when
the waveform on screen is equably and steady-going. Here this
measured value is optimal value, and the waveform at the moment
is the standard one.
 If some abnormal conditions appear on the screen during test
process, pull out the finger and reinsert to restore normal use.
 The device has an estimated lifespan of three years from the first
electrified use.
 The hanging rope attached to the device is made from Non- allergy
material, if particular group are sensitive to the hanging rope, stop
using it. In addition, pay attention to the use of the hanging rope,
do not wear it around the neck on the purpose of avoiding harm to
the patient
 This device includes a alarmfunction, users can check this according
to chapter 7.
 The device has the function of limits alarming, when the measured
data is beyond the highest or lowest limit, the device would start
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