Compare Heartsine Products
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Compare Heartsine Products
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| Device category | Public access AED | Public access AED | Public access AED |
| Waveform | SCOPE optimized biphasic escalating waveform - maintains shock effectiveness using lower joules | SCOPE optimized biphasic escalating waveform - maintains shock effectiveness using lower joules | SCOPE optimized biphasic escalating waveform - maintains shock effectiveness using lower joules |
| Max energy | 200 J | 200 J | 200 J |
| Shock types | Semi-automatic | Fully automatic | Semi-automatic |
| Time to first shock | Charge time (typical): 150 J < 8 s; 200 J < 12 s | Charge time (typical): 150 J < 8 s; 200 J < 12 s | Charge time (typical): 150 J < 8 s; 200 J < 12 s |
| Energy protocol details - Adult | 150 J, 150 J, 200 J | 150 J, 150 J, 200 J | 150 J, 150 J, 200 J |
| Energy protocol details - Paediatric | 50 J, 50 J, 50 J | 50 J, 50 J, 50 J | 50 J, 50 J, 50 J |
| Configurable Energy Protocols | - | - | - |
| Rhythm analysis + parallel charge | No: Charge time (typical): 150 J < 8 s; 200 J < 12 s | No: Charge time (typical): 150 J < 8 s; 200 J < 12 s | No: Charge time (typical): 150 J < 8 s; 200 J < 12 s |
| Pads are preconnected | - | - | - |
| Voice prompts | Yes (voice prompts and audible tones) | Yes (voice prompts and audible tones) | Yes (visual and voice prompts, CPR feedback and effectiveness monitoring) |
| Metronome | Yes | Yes | Yes |
| CPR Technology | - | - | Yes (CPR Advisor provides feedback on depth and rate, using ICG analysis) |
| 4G capability | - | - | - |
| WIFI capability | - | - | - |
| Remote monitoring platform | - | - | - |
| Alerts/notifications | - | - | - |
| IP rating | IP56 | IP56 | IP56 |
| Drop-tested | 1 m | 1 m | 1 m |
| Vibration tested | MIL STD 810F Method 514.5+, Category 4 Truck Transportation (US Highways) and Category 7 Aircraft (Jet 737 and General Aviation Exposure) | MIL STD 810F Method 514.5+, Category 4 Truck Transportation (US Highways) and Category 7 Aircraft (Jet 737 and General Aviation Exposure) | MIL STD 810F Method 514.5+, Category 4 Truck Transportation (US Highways) and Category 7 Aircraft (Jet 737 and General Aviation Exposure) |
| Display | - | - | - |
| Visual Prompts | Yes | Yes | Yes |
| Device weight | 1.1 kg (with Pad-Pak inserted) | 1.1 kg (with Pad-Pak inserted) | 1.1 kg (with Pad-Pak inserted) |
| Device dimensions | 20 cm × 18.4 cm × 4.8 cm (with Pad-Pak inserted) | 20 cm × 18.4 cm × 4.8 cm (with Pad-Pak inserted) | 20 cm × 18.4 cm × 4.8 cm (with Pad-Pak inserted) |
| Pads + battery combined cartridge | Yes (Pad-Pak integrated battery + electrodes) | Yes (Pad-Pak integrated battery + electrodes) | Yes (Pad-Pak integrated battery + electrodes) |
| Electrode life | Pad-Pak shelf life: 4 years from manufacture date | Pad-Pak shelf life: 4 years from manufacture date | Pad-Pak shelf life: 4 years from manufacture date |
| Battery life | Pad-Pak (contains pads and battery) shelf life: 4 years from manufacture date | Pad-Pak (contains pads and battery) shelf life: 4 years from manufacture date | Pad-Pak (contains pads and battery) shelf life: 4 years from manufacture date |
| Self-test/readiness | Automatic weekly self-test; status indicator shows readiness | Automatic weekly self-test; status indicator shows readiness | Automatic weekly self-test; status indicator shows readiness |
| Manual override / manual mode | - | - | - |
| Cloud/system connectivity | - | - | - |
| CardiAct Connect Compatible | Yes | Yes | Yes |
| Warranty | 8 years | 8 years | 8 years |
| Carton Qty | 8 | 8 | 8 |
| Pricing Unit | Unit/1 | Unit/1 | Unit/1 |
| Size | One Size | One Size | One Size |
| Min Order Qty | 1 | 1 | 1 |
| ARTG ID | 156690 | 228210 | 156690 |
| GMDN Code | 37805 | 48047 | 37805 |
| Medical Device Class | Class 2b | Class 2b | Class 2b |
| UNSPSC | 42172101 | 42172101 | 42172101 |
| Tax Schedule | Non-Taxable | Non-Taxable | Non-Taxable |
| Is Serialized Item | Yes | Yes | Yes |
| Is Dangerous Good | Yes | Yes | Yes |
| ARTG Intended Purpose | A device that can analyse an electrocardiogram (ECG) to determine whether or not a defibrillator shock should be delivered. It is attached to the patient through a pair of adhesive defibrillation electrodes that serve both to monitor the ECG and to deliver the defibrillator discharges. The semi-automated defibrillator indicates to the operator when to deliver the shock. | A portable electronic device designed to automatically detect cardiac arrhythmias (ventricular fibrillation/pulseless ventricular tachycardia) in a sudden cardiac arrest (SCA) patient, after which it automatically activates defibrillation of the heart through application of electrical shocks to the chest surface. It consists of an external pulse generator (EPG) with a cardiac rhythm recognition system and a pair of skin-adhesive electrodes to monitor the rhythm and deliver the shocks; it also includes a non-rechargeable battery for energy. | A device that can analyse an electrocardiogram (ECG) to determine whether or not a defibrillator shock should be delivered. It is attached to the patient through a pair of adhesive defibrillation electrodes that serve both to monitor the ECG and to deliver the defibrillator discharges. The semi-automated defibrillator indicates to the operator when to deliver the shock. |