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DIH 0300 B – USER GUIDE REANIBEX 300 6
1 INTRODUCTION
ATTENTION
POSSIBLE EQUIPMENT MALFUNCTION
• The use of cables, electrodes or batteries from other manufacturers may affect proper operation of the
equipment and invalidate the safety certification. Use only the accessories specified in this GUIDE.
• Using the REANIBEX 300 or its accessories in environmental conditions other than those specified
in this manual may affect proper operation of the equipment or the accessories. Before using the
REANIBEX 300, make sure the equipment is stabilised at the operating temperature range.
WARNING
POSSIBLE EQUIPMENT MALFUNCTION. Changing the configuration of the equipment’s factory
default values will affect the operation of the equipment. Changes to the default configuration must be
performed only by authorised personnel.
PRECAUTION
POSSIBLE DAMAGE TO THE EQUIPMENT
• Handle the patient cables and the ECG monitoring equipment carefully when using the equipment
with high frequency surgical equipment.
• The equipment can be damaged by mechanical or physical maltreatment, such as immersion in water
or falls over 0.75 m.
• The components of the equipment can undergo damage if it is placed near sources of vibration.
HAZARD
FIRE OR ELECTRICAL SHOCK HAZARD: Make sure that the accessories and all the components are
properly connected. Components or accessories that are not properly connected can cause fire or
electrical shock.
PRECAUTION
The REANIBEX 300 is intended for use in the presence of high frequency surgical equipment. After the
interferences caused by the electric scalpel, the equipment returns to its previous operating mode in 10
seconds, without losing any of the data stored. Accuracy in the measurements may be affected
temporarily during surgery with electrical equipment or defibrillation. This will not affect the safety of the
patient or the equipment. Please refer to the Instructions for Use of the electric scalpel to minimise risk
of burns in the event of a defect in the equipment.
WARNING
The REANIBEX 300 does not have the capacity to reject the pulses of internal pacemakers in all cases.
The equipment may detect pulses from internal pacemakers as QRS complexes and therefore indicate
an incorrect heart rate. Therefore, the heart rate indicated by the equipment for patients with internal
pacemakers should not be trusted.
Patients with internal pacemakers must be carefully monitored. See the “Internal pacemaker pulse
rejection” section in the Appendix of this manual. This section indicates the capacity of the equipment to
reject internal pacemaker pulses.
WARNING
The REANIBEX 300 has been designed for the treatment of cardiac arrest in adult and paediatric
patients. To apply the therapy, the REANIBEX 300 must be used with the specific electrodes indicated