1-2
non-affiliated to the manufacturer or by non-licensed personnel may affect
the safety, performance and function of the product.
When used with electrosurgery equipment, the safety of patients should be
ensured.
The patient's clinical condition and the working condition of the infusion
pump must be monitored carefully, the alarm volume and alarm levels need
to be set according to the actual needs. Operation and performance relying
solely on the auditory alarm system alone is not sufficient, and setting the
alarm at a low volume may endanger the patient. If the alarm volume is less
than the surroundings volume, which can further lead to operators identify
alarm mistakenly.
The interconnection of other infusion systems or ACCESSORIES to the
PATIENT LINE may lead to performance degradation and failure to achieve
the expected performance, the working condition of the pump and patient's
clinical condition shall be monitored regularly.
Please carefully install the power line and cables with various accessories
to prevent the patient from choking or suffocation caused by entanglement
of the cables or by electrical disturbance.
The packaging materials must be disposed of in compliance with local
laws and regulations or the hospital policy on waste management.They
must be kept out of the reach of children.
Infusion tube knots, filter coagulation and occlusions arising from needle
insertion can cause the pressure inside the infusion set to rise during
infusion. When this occurs, removing the occlusion can cause excessive
liquid to be infused into the patient, so appropriate measures should be
taken.
The pump should not be placed more than 100cm above or below the level
of the patient’s heart. The smaller the height difference between the pump,
the more accurate the pressure test in the infusion cannula will be.
It is recommended that infusion pump with conventional infusion sets is
used with infusion sets recommended by manufacturers (please refer to
6.10.1 Infusion Pump with Conventional Infusion Sets for specific brands).
When use of non-recommended infusion sets, please make sure to confirm
relevant infusion performance (such as accuracy, air bubble and pressure)
on infusion pump, and contact the company for calibration service. Air
bubble calibration, Accuracy Calibration and Pressure Calibration shall be
performed sequentially, the infusion sets can only be used after
confirmation, otherwise Mindray Scientific is not responsible for infusion
performance (such as accuracy, air bubble and pressure) and relevant
alarm function of the infusion pump. Its accuracy cannot be guaranteed
when the pump is used with an infusion set without calibration.
Summary of Contents for BeneFusion VP5
Page 1: ...BeneFusion VP5 BeneFusion VP5 Ex BeneFusion VP5 Neo Infusion Pump Operator s Manual ...
Page 2: ......
Page 83: ...A 12 Unit of Rate ml h ...
Page 102: ...F 1 F Declaration of Conformity P N 046 013877 00 1 0 ...
Page 103: ......
Page 104: ......