Bexen REANIBEX 300, Руководство пользователя

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DIH 0300 B – USER GUIDE REANIBEX 300 5
1 INTRODUCTION
WARNING
• Carefully follow the instructions indicated on the labels of the defibrillation and the monitoring
electrode pads.
• The defibrillation and monitoring electrode pads must be used before the expiry date indicated on their
labels. If the electrode pads are dried out or damaged, they can generate electrical arcs and burns
during their use.
• Do not open the defibrillation electrode pad packaging until just prior to use.
• Do not reuse the defibrillation or monitoring electrode pads. Dispose of all defibrillation or monitoring
electrode pads after use.
WARNING
• Keep careful watch over the patient during defibrillation. A delay in delivering the shock can involve a
spontaneous change from a rhythm analysed as shockable to a rhythm that is not shockable, giving
rise to inadequate shock delivery.
ATTENTION
POSSIBLE DAMAGE TO THE EQUIPMENT. Before using the defibrillator, disconnect the patient from
all the equipments that are not protected against defibrillation.
WARNING
POSSIBLE ELECTRICAL INTERFERENCE
• The presence of radio frequency (RF) sources near the REANIBEX 300 can cause incorrect operation
of the equipment. The electromagnetic compatibility of adjacent equipment must be verified before
using the REANIBEX 300.
• Avoid using the REANIBEX 300 placed next to or on other equipment. If the equipment must be used
next to or on other equipment, make sure that the equipment works properly before using it on a
patient.
• The REANIBEX 300 is intended to be used exclusively by medical personnel. The equipment can
cause radio interferences or interfere with the operation of adjacent equipment. It may be necessary to
mitigate these effects by reorienting or moving the REANIBEX 300 equipment or shielding the location.
• The use of cables, electrodes or accessories not specified in this manual for use with the REANIBEX
300 can give rise to an increase in emissions or lower immunity versus electromagnetic or radio
interferences. These interferences can affect operation of the defibrillator or of equipment in the
immediate surroundings.
• The REANIBEX 300 must be installed and started up according to the information dealing with
Electromagnetic Compatibility (EMC) in Section “A.6 - Electromagnetic Compatibility Guide”.
WARNING
• The REANIBEX 300 and its accessories may be sensitive to interferences from other sources of
emissions.
ATTENTION
RESTRICTIONS FOR USE. ECG and monitored parameter waveform artefacts caused by
electromagnetic interference should be evaluated by a physician or staff authorised by a physician to
determine whether they could adversely affect patient diagnosis or treatment.