The HeartSine Samaritan® PAD 350P is an affordable semi-automated AED
with voice instruction and CPR rate assistance. It is lightweight (2.4 lbs) with an IP56 rating for durability.
Sudden Cardiac Arrest (SCA) is a leading cause of death globally. Response time is critical for survival. The HeartSine Samaritan® PAD 350P was designed especially for use in public areas by providing a sophisticated defibrillator for adult or pediatric use, inside a lightweight and easy-to-operate system.
Portable and lightweight
The Samaritan PAD is lighter (2.4 lbs.) and smaller than other defibrillators.
Durable
The Samaritan PAD 350P resists shock and vibration and carries an IP56 Rating, the industry's highest rating against dust and water. It also carries a 10-year unit warranty.
Advanced Technology
The Samaritan PAD 350P utilizes proprietary electrode technology, advanced and stable firmware, and proprietary SCOPE™* Biphasic Technology (an escalating and low-energy waveform that automatically adjusts for patient impedance differences) to assess rhythm and recommend defibrillation if necessary.
Easy-to-Follow Visual and Verbal Guides
The Samaritan PAD 350P features easy to understand visual and voice prompts that guide a user through the process.
Two Button Operation
Only two buttons, ON/OFF and SHOCK, are required, providing straightforward operation.
Always Ready
A System Status Ready Indicator flashes to show that the complete system is operational and ready for use. Device automatically runs self check each week.
| Specifications | |
|---|---|
| Physical (With Pad-Pak™ Inserted) | |
| Size | 8.0 in x 7.25 in x 1.9 in (20 cm x 18.4 cm x 4.8 cm) |
| Weight (including Pad-Pak Battery) | 2.4 lbs (1.1 kg) |
| Defibrillator | |
| Waveform | Self-Compensating Output Pulse Envelope (SCOPE) Biphasic waveform. Optimized biphasic escalating waveform compensates energy, slope and envelope for patient impedance. |
| Energy Selection | |
| Adult | Shock 1: 150J; Shock 2: 150J; Shock 3: 200J |
| Pediatric | Shock 1: 50J; Shock 2: 50J; Shock 3: 50J |
| Charging Time | |
| New Battery | Typically 150J in < 8 seconds, 200J in < 12 seconds |
| After Six Discharges | Typically 150J in < 8 seconds, 200J in < 12 seconds |
| Patient Analysis System | |
| Method | Evaluates patient’s ECG, signal quality, electrode contact integrity and patient impedance to determine if defibrillation is required. |
| Sensitivity/Specificity | Meets ISO 60601-2-4 |
| Environmental | |
| Operating/Standby Temperature | +32°F to +122°F (0°C to 50°C ) |
| Temporary Transportation Temperature | 14°F to 122°F (–10°C to 50°C) for up to two days. Unit must be returned to standby/operating temperature for 24 hours before use. |
| Relative Humidity | 5 to 95 (non-condensing) |
| Water Resistance | IEC 60529/EN 60529 IP56 |
| Altitude | 0 to 15,000 feet (0 to 4,575 meters) |
| Shock | MIL STD 810F Method 516.5, Procedure I (40G’s) |
| Vibration | MIL STD 810F Method 514.5+ - Category 4 Truck Transportation, US Highways - Category 7 Aircraft, Jet 737 & General Aviation (Exposure) |
| EMC | EN 60601-1-2 |
| Radiated Emissions | EN55011 |
| Electrostatic Discharge RF Immunity | EN61000-4-3 80MHZ-2.5GHZ (10V/m) |
| Magnetic Field Immunity | EN61000-4-8 (3 A/m) |
| Aircraft | RTCA/DO-160F, Section 21 (Category M) |
| Falling Height | 3.3 feet (1 meter ) |
| Event Documentation | |
| Type | Internal Memory |
| Memory Capacity | 90 minutes of ECG (full disclosure) and event/incident recording |
| Playback Capabilities | Custom USB cable directly connected to PC and Saver™ EVO Windows-based data review software |
| Materials Used | |
| Housing | ABS, Santoprene |
| Electrodes | Hydrogel, Silver, Aluminum and Polyester |
| Pad-Pak — Electrode and Battery Cartridge | |
| Shelf Life | Four years from manufacture date |
| Weight | 0.44 lbs (0.2 kg) |
| Size | 3.93 in x 5.24 in x .94 in (10 cm x 13.3 cm x 2.4 cm) |
| Battery Type | Lithium Manganese Dioxide (LiMnO2) |
| Capacity | > 60 shocks at 200J (18V, 1.5 Amp Hrs) |
| Electrodes | HeartSine Samaritan disposable defibrillation pads are supplied as standard with each device |
| Placement | Anterior-lateral (Adult); Anterior-posterior (Pediatric) |
| Active Gel Area | 15.5 in2 (100 cm2) |
| Cable Length | 3.3 feet (1 meter) |