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ZOLL R Series Service Manual

ZOLL R Series
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Warnings
9650-0912-01 Rev. N ZOLL R Series Operator’s Guide 1–15
The R Series should be installed and put into service according to the EMC information in
Appendix A of this manual.
Assess the Wi-Fi performance for the possibility of RFI in your environment of use.
If multiple devices are transmitting simultaneously to the same access point, Wi-Fi data transfer
will be slowed down. If the access point is too overloaded, data transmission failures can occur.
The use of accessories, transducers, and cables other than those specified in this manual and
related R Series option manual inserts may result in increased emissions or decreased immunity
of the R Series.
Do not use or place the unit in service if the Code Readiness indicator (at the upper right of the
front panel) displays a red “X”.
Carefully route patient cables to avoid tripping over them, or inadvertently pulling the unit onto
the patient.
Always inspect the unit for damage if it has been dropped.
To avoid risk of electric shock, this equipment must only be connected to a supply mains with
protective earth.
Do not modify this equipment without authorization from the manufacturer.
Ensure that the unit is always positioned so as to allow unobstructed access to and detachment
of the power cord from the unit to AC mains.
ECG Analysis, Defibrillating, Pacing and CPR
Prior to attempting synchronized cardioversion, ensure the ECG signal quality is good and that
sync markers are displayed above each QRS complex.
Do not use the unit in advisory mode during patient movement. A patient must be motionless
during ECG rhythm analysis. Do not touch the patient during analysis. If transporting the
patient, cease all movement before beginning ECG analysis.
ECG rhythm analysis does not warn of patient asystole, which is not a shockable rhythm.
The ECG rhythm analysis function might not reliably identify ventricular fibrillation in the
presence of an implanted pacemaker. Inspection of the electrocardiogram and clinical evidence
of cardiopulmonary arrest should be the basis for any treatment of patients with an implanted
pacemaker.
Implanted pacemakers might cause the heart rate meter to count the pacemaker rate during
incidents of cardiac arrest or other arrhythmias. Dedicated pacemaker detection circuitry may
not detect all implanted pacemaker spikes. Check the patient's pulse; do not rely solely on heart
rate meters. Patient history and physical examination are important factors in determining the
presence of an implanted pacemaker. Pacemaker patients should be carefully observed.
Do not place electrodes directly over an implanted pacemaker.
The R Series unit detects ECG electrical signals only. It does not detect a pulse (effective
circulatory perfusion). Always verify pulse and heart rate by physical assessment of the patient.
Never assume that the display of a nonzero heart rate means that the patient has a pulse.
To avoid possible damage to the R Series unit, turn off pacing before defibrillating the patient
with a second defibrillator.
Do not use the unit’s ECG-out signal as a synchronization pulse for another defibrillator or
cardioverter.

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ZOLL R Series Specifications

General IconGeneral
Defibrillator TypeManual and AED
PacingYes
ECG MonitoringYes
SpO2 MonitoringYes
FAST-SpO2Yes
IP RatingIP55
Defibrillator WaveformBiphasic
Energy Levels1-360 Joules
DisplayLCD
Pacer TypeDemand
Pacer Rate30-180 ppm
Pacer Output0 – 140 mA
EtCO2 MonitoringOptional
NIBP MonitoringOptional
Temperature MonitoringOptional
PrinterIntegrated
Battery TypeLithium-ion
CPR FeedbackYes
Data StorageInternal memory
ConnectivityUSB

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