ZOLL E Series Monitor Defibrillator Rev R - Manual (Page 19)

General Information
9650-1210-01 Rev. R 1-11
Safety Considerations
The E Series products are high energy devices capable of delivering up to 200 joules. To completely deactivate the
device, you must turn the selector switch to the OFF position.
• In order to disarm a charged defibrillator, do one of the following: Turn the selector switch to MONITOR, OFF or
PACER (pacer equipped versions only)
• Change the selected defibrillator energy
As a safety feature, the device automatically disarms if left charged for more than 60 seconds (15 seconds for AED
versions).
WARNINGS - General
• Federal (U.S.A.) law restricts this device to use by or on the order of a physician.
• The use of external pacing/defibrillation electrodes or adapter devices from sources other than ZOLL is not
recommended. ZOLL makes no representations or warranties regarding the performance or effectiveness of its
products when used in conjunction with pacing/defibrillation electrodes or adapter devices from other sources.
Device failures attributable to the use of pacing/defibrillation electrodes or adapters not manufactured by ZOLL may
void ZOLL's warranty.
• Proper operation of the unit, together with correct electrode placement, is critical to obtaining optimal results.
Operators must be thoroughly familiar with proper device operation.
• Do not use the unit in Semiautomatic mode during patient movement. A patient must be motionless during ECG
analysis. Do not touch the patient during analysis. Cease all movement via stretcher or vehicle before analyzing the
ECG. If using the device in an emergency vehicle, bring the vehicle to a halt before using in Semiautomatic mode.
• Place the patient on a firm surface before performing CPR.
• The device is protected against interference from radio frequency emissions typical of two-way radios and cellular
phones (digital and analog) used in emergency service/public safety activities. Users should assess the device’s
performance in their typical environment of use for the possibility of radio frequency interference from high-power
sources. Radio Frequency Interference (RFI) may be observed as shifts in monitor baseline, trace compression,
display brightness changes or transient spikes on the display.
• E Series units equipped with the Bluetooth® option include an RF transmitter which transmits with 7dBm/5mW
power in the 2.4 GHz ISM band.
• Do not operate the unit without a battery during patient care. Keep a fully charged spare battery pack with the
device at all times.
• Regular use of partially charged battery packs without fully recharging between uses results in permanently
reduced capacity and early battery pack failure.
• Test batteries regularly. Batteries that do not pass ZOLL’s capacity test could unexpectedly shutdown without
warning.
• Replace the battery with a fully charged battery immediately after the LOW BATTERY or REPLACE BATTERY
message.
• Emergency defibrillation should be attempted only by appropriately trained, skilled personnel who are familiar with
equipment operation. Training appropriateness, such as Advanced Cardiac Life Support (ACLS) or Basic Life
Support (BLS) certification, should be determined by the prescribing physician.
• Synchronized cardioversion should only be attempted by skilled personnel trained in Advanced Cardiac Life
Support (ACLS) and familiar with equipment operation. The precise cardiac arrhythmia must be determined before
attempting defibrillation.
• Prior to attempting synchronized cardioversion, ensure that the ECG signal quality is good and that sync marks are
displayed above each QRS complex.
• Pacing must be turned off before defibrillating with a second defibrillator. Otherwise, the E Series unit may be
damaged.
• Carefully route the patient cables to avoid tripping over them.
• Carefully route the patient cables to avoid inadvertently pulling the unit onto the patient.
• Do not carry the unit while in use.
• These operating instructions describe the functions and proper operation of the E Series products. They are not
intended as a substitute for a formal training course. Operators should obtain formal training from an appropriate
authority prior to using the device for patient care.
• Do not disassemble the unit. A shock hazard exists. Refer all problems to authorized service personnel.