PULOX ABDM50 Manuel D'instruction page 46

protected against electric shock. When high frequency or defibrillation
devices are applied to the patient, no special precautions need to be
taken and the defibrillator discharge will not affect the device.
- If Luer lock connectors are used in the construction of tubing, there is a
possibility that they might be inadvertently connected to intravascular
fluid systems, allowing air to be pumped into a blood vessel.
- This device is suitable for occasions with electrosurgical equipment, but
when used with electrosurgical equipment, patient safety must be given
the highest priority.
- When the monitor is wetted, please stop using it and contact us.
- After pressing the power button, if the device has display fault such as
white screen, blurred screen or no display content, please contact our
company.
Note
A. The software was developed in accordance with IEC60601-1. The possibil-
ity of hazards arising from errors in the software program has been mini-
mized.
B. All analog and digital equipment connected to this device must be certified
to IEC standards (such as IEC60950: Information technology equipment-
Safety and IEC60601-1: Medical electrical equipment-Safety), and all equip-
ment should be connected to in accordance with the requirement of the valid
version of the IEC60601-1-1 system standard. The person connecting the ad-
ditional equipment to the signal input and output port is responsible for
whether the system complies with the IEC60601-1 standard.
C. Refer to the following chapters for the minimum value of patient physio-
logical signals. Operation of the device below the minimum value may result
in inaccurate results.
D. The Monitor shall comply with the standard IEC 80601-2-30: Particular re-
quirements for basic safety and essential performance of automated non-
invasive sphygmomanometers.
1.2 General Information
This device is defibrillator protected; the time of defibrillation recovery is 5
seconds. Note that no precautions specific to the device is required during
defibrillation, and defibrillation discharge has no effect on the monitor. The
equipment uses the gray silicone airway, in case of the effect to the equip-
ment when defibrillation device was used on the patient.
General instruction:
The device is applied to Blood Pressure (BP) measure and monitor for adult
(including pregnant women), pediatric, and neonatal. It most stores 300 rec-
ords of common user and 350 of ambulatory Blood Pressure data. Every rec-
ord includes the detailed measure time, systolic blood pressure, diastolic
blood pressure, mean blood pressure, pulse rate, error message and record
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