Product Manual

Technical Data
Table 3: Functionality
Parameter Detail
RHYTHMx®
ECG analysis
performance
The AED RHYTHMx ECG Analysis system analyzes
the patient’s ECG and advises you when the AED
detects a shockable or non-shockable rhythm.
This system makes it possible for a person, with
no training in the interpretation of ECG rhythms,
to oer debrillation therapy to victims of
sudden cardiac arrest.
Waveform STAR® Biphasic
Impedance 25 Ω to 175 Ω
Energy
(preinstalled pads,
model number
XELAED001)
Escalating energy from 95 J to 354 J
Energy
(pediatric pads,
model number
XELAED003)
Escalating energy from 22 J to 82 J
Shock times • Initiation of rhythm analysis to ready to shock:
15 seconds (typical); 45 seconds (maximum)
With a fully charged battery
• Initiation of rhythm analysis to ready to shock,
used battery: 15 seconds typical); 45 seconds
(maximum) with a battery that has been used
for 15 shocks
• Lid-open to ready to shock: 15 seconds (typical)
With a battery that has been used for 15 shocks
• Post CPR to ready to shock: 10 seconds (typical)
With these conditions: “Post CPR” begins
after the “Stop CPR” prompt is given; English
is the selected language; semi-automatic AED
detects persistent VF; new, unused battery is
attached to the AED.
Automated
self-tests
• Daily: Battery, pads, internal electronics, but-
tons.
• Weekly (every 7 days): Battery, pads, CPR feed-
back device accelerometer, internal electronics,
buttons, high voltage circuit (standard tests,
partial energy charge cycle).
• Monthly (every 28 days): Battery under load,
pads, CPR feedback device accelerometer, in-
ternal electronics, buttons, high voltage circuit
(advanced tests, full energy charge cycle).
Audible alerts • Voice prompts
• Maintenance alerts
Indicators • Battery status
• Check pads
• Rescue Ready
• Service
• Text display
USB port
communication
Event download, device data, conguration, and
maintenance
Parameter Detail
Internal data
storage
90 minutes
Table 4: Applicable standards
Type Detail
Cardiac Science AEDs have been designed and manufactured to
conform to the highest standards of safety and performance includ-
ing electromagnetic compatibility (EMC). This AED and debrillation
pads conform to the applicable requirements of the following:
General • CE Marked by BSI 0086 per
the Medical Device Directive
93/42/EEC.
• Classied by CSA with respect
to electric shock, re and
mechanical hazards only in
accordance with CAN/CSA C22.2
No. 60601-1:08, EN60601-1 and
EN60601-2-4.
• Certied to CAN/CSA Standard C22.2 No.
60601-1:08 and 60601-2-4.
Safety and
performance
• IEC 60601-1
• IEC 60601-1-2
• IEC 60601-2-4
• RTCA DO-160G:2010: Section 5 Category C;
Section 4, Category A4
• EN 1789
Emissions EM: EN 55011+A1/CISPR 11, Group 1, Class B
Immunity • EM
• IEC 61000-4-3, Level X, (20V/m)
• IEC 60601-2-4 (20V/m)
• Magnetic
• IEC 61000-4-8
• IEC 61000-4-8
• ESD
• IEC 61000-4-2
• IEC 60601-2-4
• 6 KV contact discharge, 8 KV air gap discharge
Free fall drop MIL-STD-810G, Method 516.5, Procedure IV
Shock MIL-STD-810G 516.5, Procedure 1
Vibration
(Random)
MIL-STD-810G, Method 514.5, Procedure 1,
Category 24; RTCA DO-160G, Section 8,
Category S, Zone 2 (curve B) and Category U,
Zone 2 (curves F and F1)
Vibration (Sine) MIL-STD-810G, Method 514.5, Procedure 1,
Category 24, Helicopter Minimum Integrity
Enclosure
protection
IEC 60529, IP55
Table 3: Functionality (Continued)
B-2 Powerheart® G5 Automated External Debrillator70-01704-01 B