Equipped with Real CPR Help technology when used with the CPR-D padz, to assist first responders with performing high quality CPR.
- CPR coaching and real-time feedback with use of the CPR-D Padz®
- Lid designed to be placed under a victim’s shoulders to optimize an open airway
- Uses consumer lithium 123A batteries
- Single piece electrode pads
- Energy Selection: Adult Pad-Pak 120J > 150J > 200J | Paediatric-Pak 50J > 70J > 85J
- LCD text prompts
Available unit options:
Fully-automatic Defibrillator: Automatically shocks the patient if a shockable heart rhythm is detected.
Semi-automatic Defibrillator: Shock button is required to be pushed if a shockable heart rhythm is detected.
Waveform: Rectilinear Biphasic
Defibrillator Charge Hold Time: 30 seconds
Energy Selection: Automatic preprogrammed selection (120J, 150J, 200J)
Patient Safety: All patient connections are electrically isolated
Charge Time: Less than 10 seconds with new batteries
Electrodes: ZOLL CPR-D-padz, pedi-padz® II or stat-padz® II
Self-test: Configurable automatic self-test from 1 to 7 days.
Default = every 7 days. Monthly full-energy test (200J).
Automatic Self-Test Checks: Battery capacity, electrode connection, electrocardiogram and charge/discharge circuits, microprocessor hardware and software, CPR circuitry and CPR-D sensor, and audio circuitry
CPR: Metronome Rate: Variable 60 to 100 CPM
Depth: 3/4″ to 3.5″; 1.9 to 8.9 cm
Defibrillation Advisory: Evaluates electrode connection and patient ECG to determine if defibrillation is required
Shockable Rhythms: Ventricular fibrillation with average amplitude >100 microvolts and wide complex ventricular tachycardia with rates greater than 150 BPM for adults, 200 BPM for pediatrics.
For ECG Analysis Algorithm sensitivity and specificity, refer to AED Plus Administrator’s Guide.
Patient Impedance Measurement Range: 0 to 300 ohms
Defibrillator: Protected ECG circuitry
Display Format: Optional LCD with moving bar
Size: 2.6″ x 1.3″; 6.6 cm x 3.3 cm
Optional ECG Viewing Window: 2.6 seconds
Optional ECG Display Sweep Speed: 25 mm/sec; 1″/sec
Battery Capacity: Typical new (20°C) = 5 years (225 shocks) or 13 hours continuous monitoring. End
of life designated by Red X (typical remaining shocks = 9).
Data Recording and Storage: 50 minutes of ECG and CPR data. If audio recording option is installed and enabled, 20 minutes of audio recording, ECG, and CPR data. If audio recording is disabled, 7 hours of ECG and CPR data.
PC Minimum Requirements For Configuration and Patient Data Recovery: Windows® 98, Windows® 2000, Windows® NT, Windows® XP, Windows® 7, IBMcompatible PII with 16550 UART (or higher) computer. 64MB RAM. VGA monitor or better. CD-ROM drive. IrDA port. 2MB disk space.
Size: (H x W x D) 5.25″x 9.50″ x 11.50″; 13.3 cm x 24.1 cm x 29.2 cm
Weight: 6.7 lbs; 3.1 kg
Power: User-Replaceable Batteries. 10 Type 123A Photo Flash lithium manganese dioxide batteries
Device Classification: Class II and internally powered per EN60601-1
Design Standards: Meets applicable requirements of UL 2601, AAMI DF-39, IEC 601-2-4, EN60601-1, IEC60601-1-2
Operating Temperature: 32° to 122°F; 0° to 50°C
Storage Temperature: -22° to 140°F; -30° to 60°C
Humidity: 10 to 95% relative humidity, non-condensing Vibration: MIL Std. 810F, Min. Helicopter Test
Shock: IEC 68-2-27; 100G
Altitude: -300 to 15,000 ft.; -91m to 4573 m
Particle and Water Ingress: IP-55
Shelf Life: 5 years
Conductive Gel: Polymer Hydrogel
Conductive Element: Tin
Packaging: Multilayer foil laminate pouch
Impedance Class: Low
Cable Length: 48 in (1.2 m)
Sternum: Length: 6.1 in (15.5 cm); Width: 5.0 in (12.7 cm); Length, conductive gel: 3.5 in (8.9 cm); Width, conductive gel: 3.5 in (8.9 cm); Area, conductive gel: 12.3 sq in (79.0 sq cm)
Apex: Length: 6.1 in (15.5 cm); Width: 5.6 in (14.1 cm); Length, conductive gel: 3.5 in (8.9 cm); Width, conductive gel: 3.5 in (8.9 cm); Area, conductive gel: 12.3 sq in (79.0 sq cm)
Complete Assembly: Folded Length: 7.6 in (19.4 cm); Folded width: 7.0 in (17.8 cm); Folded height: 1.5 in (3.8 cm)
Design Standards: Meets applicable requirements of ANSI/AAMI/ISO DF-39-1993 ZOLL Medical Corporation