Specifications
LIFEPAK 1000 Defibrillator Operating Instructions A-7
©2018 Physio-Control, Inc.
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)
Drop • 18-inch drop onto each surface, repeated 5 times each, 30
drops total
• EN 1789 0.75 meter drop onto each surface, 6 drops total
• MIL-STD-810F, 516.5 Procedure IV, 1 meter drop on each
corner, edge, and surface
Vibration MIL-STD-810F, Method 514.5, Category 20 Ground Vehicle:
Random vibration test, 1 hour per axis, 3.15g rms
EMC For EMC information, refer to the Electromagnetic Compliance
Guidance provided with the device.
Physical Characteristics
Weight 3.2 kg (7.1 lb) with nonrechargeable battery and REDI-PAK
electrodes
Height 8.7 cm (3.4 in.)
Width 23.4 cm (9.2 in.)
Depth 27.7 cm (10.9 in.)
Data Storage
Memory Capacity • Dual patient storage
• Minimum of 40 minutes of ECG for the current patient
• Summarized data stored for the previous patient
Report Types • Continuous ECG—Continuous patient ECG report
• Summary—Summary of critical resuscitation events and
associated ECG waveforms
• Event Log report—Report of time-stamped markers reflecting
operator and device activity
• Test Log report—Device self-test activity report
Capacity Minimum 100 time-stamped event log entries
Data Review CODE-STAT 6.0 (minimum) or DT EXPRESS 2.0 (minimum)
software
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