Cardiac Science Powerheart G5 Pediatric Reusable Training Pads

Powerheart-G5-Pediatric-Reusable-Training-Pads

Additional Images

  • Powerheart-G5-Pediatric-Reusable-Training-Pads

Cardiac Science Powerheart G5 Pediatric Reusable Training Pads

Product Code XTRPAD003AUSA

0 reviews

In Stock

What's Included?

  • 1 set of G5 Pediatric training pads

Designed for use with the G5 AED training unit, these reusable pediatric pads will enable you to demonstrate to your learners a realistic rescue process and the difference in the procedure if it were a child needing treatment for sudden cardiac arrest. 

For use with Cardiac Science’s Powerheart G5 AED Training Unit, the reusable pediatric training electrode pads allow trainers to highlight the differences between treating an adult and child in cardiac arrest.

Unlike their clinical counterparts, these electrode pads are reusable, however, this is the only difference between the two. They also assist the learner in understanding where to place the pads on the child as well as how the commands from the AED may change after the pediatric pads have been attached. 

Key Features

  • Designed for exclusive use with the Powerheart G5 AED training unit
  • Enables the AED training unit to showcase pediatric treatment for sudden cardiac arrest
  • Almost identical in design to boost the learner’s confidence and understanding of the electrode pads
  • Clear and easy to understand instructional diagrams to help the responder to place the pads correctly 
  • Can be used with any training manikin in any training scenario

How to use

Functioning in the exact same way as the clinical electrode pads for the Powerheart G5 AED, the pediatric pads enable learners to thoroughly understand how the AED would function if a real-life paediatric, cardiac emergency occurred.

The instructional diagrams offer learners a simple yet effective training experience. These diagrams indicate where they should be placed, as pediatric pad placement differs from adult pad placement. Understanding this can help save vital time in the moments that follow a cardiac arrest.

More Information

If you would like more information about the Powerheart G5 Reusable Pediatric Training Pads, the defibshop team are the ones with the answers.

Call us on 800 989 7768 and one of our friendly, knowledgeable advisors will be happy to assist with any of your queries.

 

 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.