Powerheart AED Patient Simulator

Powerheart AED Patient Simulator

Product Code 9021-002USA

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What's Included?

  • AED Patient simulator

Designed for use with Cardiac Science’s Powerheart G3 AED range, including the G3 Pro, this AED Patient Simulator can switch a live, clinical AED into a training model to demonstrate to users the different stages of a cardiac arrest rescue process. 

The simulator can program the users G3 to display the analysis of a patient’s heart stage with various arrhythmias. This helps the learners to understand how the AED will react in different circumstances.

Programmable Waveforms

  • Over 200bpm- VF – Ventricular Fibrillation
  • Approx 185bpm- VT fast – Ventricular Tachycardia  
  • Approx 140bpm - VT slow – Ventricular Tachycardia
  • Approx 72bpm - NSR – Normal Sinus Rhythm –– ‘non-shockable’ rhythm
  • ASYS – Asystole – Non-shockable rhythm
  • Approx 170bpm - SVT slow – Supra Ventricular Tachycardia  
  • Artifact – Unusable signal, heart rate not applicable
  • 210bpm Approx - SVT fast – Supra Ventricular Tachycardia  

How to use

Simply connect your Powerheart G3 AED and you will be able to treat the unit as a training unit, enabling you to teach other users how to use an AED properly and with confidence.

The multiple waveform capabilities allow the AED to mirror a real rescue. This allows students to thoroughly understand what needs to be done for patients experiencing different heart rhythms and how the AED will react to the different arrhythmias.

More Information

If you would like to learn more about the AED Patient Simulator, or any of our other products, the friendly and informative defibshop team are here to help.

To get in contact with one of our advisors, simply call 888 820 0760 and they’ll be happy to share their knowledge with you and help you in any way they can.


 Want to know why you should choose us? 

  • Experienced and knowledgeable staff on-hand to offer impartial advice on all things AEDs
  • We have a nationwide training network to deliver training in the use of a defib and CPR
  • Not only providing free battery and pad reminders, we also will replace your electrode pads for free if you use your defib in the first two years after purchase
  • Over 14 years worth of experience as an AED specialist 
  • 5 / 5 Review Score
  • Over 97% of our customers would buy from us again


What is an IP rating?

An IP (Ingress Protection) rating classifies the degrees of protection of an electrical item against water and dust. Beginning with IP and followed by two numbers, the first digit is indicative of the item’s resistance to dust and the second is of its resistance to water. Protection against dust is measured from */ 0 up to 6, whereas protection against water is measured from */ 0 up to 8. The protection against these elements increases as the number does, with * / 0 telling us that the item has NO protection against either dust or water.

Why is this important?

The IP rating of a defib will tell you (and us!) whether it is suitable for the environment where it’s most likely to be used; for example, if there is a good chance your defib may be used in an outdoor environment, you will need a unit with a higher IP rating to ensure it can be used regardless the weather or terrain. If you are looking for a defibrillator more suitable for an indoors environment, you can afford to choose one with a lower IP rating, based on the other features that may be more suitable.

When a particular product is “approved” by the FDA, this marks the pass in the premarket approval (or PMA) application of a particular product which has been submitted to the FDA.

To receive approval of a device through a PMA application, the applicant in question must provide reasonable assurance of the device’s safety and effectiveness which is then challenged by the FDA before being approved.

Whilst all AEDs can be used to increase chances of survival and even save a life in the event of a cardiac arrest, FDA approved devices provide that extra piece of mind that the specific unit being used has undergone vigorous and substantial testing to ensure that that particular piece of equipment operates just as it should and provides the most effective care possible.

Many manufacturers perform their own tests on products, but not all defibrillators will undergo the same premarket approval as FDA approved devices and there is no guarantee or stamp of certification if testing has taken place with non-FDA approved products.