Cardiac Science Powerheart G3 Pediatric Training Pads


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  • Powerheart-G3-Pediatric-Training-Pads

Cardiac Science Powerheart G3 Pediatric Training Pads

Product Code 9725-001USA

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What's Included?

  •  Powerheart G3 AED pediatric training pads (one pair)

Designed to be used with the G3 Training Unit; these training pediatric pads will enable you to simulate a realistic rescue process for your learners, so they can effectively understand what action needs to be taken in an emergency. 

The pediatric pads are designed to provide learners with the knowledge of how to use a life-saving AED on a child between the ages of 1-8.

The primary difference between adult and pediatric electrode pads is the level of joules delivered in defibrillation. The output is set to a safer level for that of a child’s heart and are placed differently for effective treatment.

Key Features

  • Designed for exclusive use with the Powerheart G3 Training Unit
  • Clear and easy to understand diagrams help learners to place electrode pads correctly on a manikin
  • Provides learners with a realistic training scenario
  • Learners can see and understand the difference between adult and child pads

How to use

These training units are for use with the G3 Training Unit and work similarly to that of a clinical device. The pediatric pads will allow trainees to practice effective pad placement and how to administer treatment to a child who has suffered a cardiac arrest.

The pads have clear, easy to understand images on the electrodes to help learners place the training pads correctly on the manikin or victim, they are designed to be the same as their medical counterparts which would actually be used should a real emergency occur. 

More Information

If you would like to learn more about the Pediatric Training Pads which are designed for Cardiac Science’s G3 AED range, the defibshop team are always on hand to help.

With over a decade’s worth of knowledge of everything  AED, our team is sure to match you to your perfect product. Give them a call on 800 989 7768. 


 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.