PULOX PO-300 Mode D'emploi page 23

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Please don't measure this device with functional tester for the device's
related information.
1.3 Attention
 Keep the oximeter away from dust, vibration, corrosive substances,
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 (7.1) for
instructions of cleaning and disinfection.
 Do not immerse the oximeter in liquid. When it needs cleaning, please
wipe its surface with disinfectant solution using a soft cloth. Do not spray
any liquid directly onto the device.
 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.
 The update period of data is less than 5 seconds, which is changeable
according to different individual pulse rate.
 Please read the measured value when the waveform on screen is
equably and steady-going, 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 an alarmfunction, users can check this according to
chapter 6 as a reference.
 The device has the function of limits alarming, when the measured data
is beyond the highest or lowest limit, the device would start alarming
automatically on the premise of the alarming function is on.
 The device may not work for all patients. If you are unable to achieve
EN