Physio-Control LIFEPAK 1000 - Manual (Page 56)

Specifications
A-6 LIFEPAK 1000 Defibrillator Operating Instructions
Waveform Amplitude 1 cm/mV, nominal
Display Range Differential: ±1.4 mV full scale, nominal
Heart Rate 20 to 300 BPM digital display.
Display "---" if heart rate is less than 20 BPM.
Heart symbol flashes for each QRS detection
Displayed ECG ECG information is received from therapy pads in anterior-lateral
or anterior-posterior positions, or from the 3-wire ECG cable in
Lead II.
Controls
On/Off Controls device power
Shock Controls the delivery of defibrillation energy
Soft Keys Used during device setup and during patient use: Analyze,
Charge, Disarm
Menu button Used to access additional device features
Readiness Display
The readiness display shows device status
OK Indicator Indicates OK when the last self-test was completed successfully.
Battery Capacity
Indicator Segmented display showing battery capacity
Service Indicator Service required when displayed
Environmental
Note: All performance specifications defined assume that the device has been stored
(two hours minimum) at the operating temperature prior to operation.
Operating
Temperature 0° to 50°C (32° to 122°F)
One-Hour Operating
Temperature From room temperature to temperature extreme, one-hour
duration:
-20° to 60°C (-4° to 140°F)
Storage Temperature With nonrechargeable (Li/MnO
2
) battery and electrodes, maximum
exposure time limited to seven days: -30° to 60°C (-22° to 140°F)
Atmospheric
Pressure 575 hPa to 1060 hPa, 4572 to -382 meters (15,000 feet to -1250
feet)
Relative Humidity 5% to 95% (noncondensing)
Dust/Water IEC 60529 IP55 with battery and REDI-PAK electrodes installed
Shock MIL-STD-810F, Method 516.5, Procedure 1, (40g peak, 15–23
msec pulse, 45 Hz crossover frequency)
Bump EN 1789 and IEC 60068-2-29, Test Eb: (1000 bumps, 15g, 6 ms,
vertical direction)