Defibtech Pediatric Training Pad Package (5 sets)


Additional Images

  • defibtech-paediatric-training-package-5-sets

Defibtech Pediatric Training Pad Package (5 sets)

Product Code DDP-205TR

0 reviews

In Stock

What's Included?

  • Pediatric training pads (Pack of 5)

These non-functional replacement paediatric training electrode pads will prepare learners for responding to a real cardiac emergency.

Responding to an emergency situation can be extremely stressful which is why having confidence in using an AED is essential, training pads will help you familiarize the steps and become confident in the correct placement of the pads

Enhancing the Training Experience

For use with the Defibtech training units, a pack of 5 pads ensure you are well stocked up and multiple learners are able to practice using the equipment.

Being able to provide effective and realistic training is vital for helping to create effective and prompt first aiders. These pads will allow learners to become familiarized with the placement of pads and how they work when connected with an AED.

Correct pad placement is necessary to increase the victim's chance of survival and it is important to remember that electrode pads are placed differently on children than they are on adults. These pads will allow the learner to practice this and become familiar with all of the steps.

More Information

Want to learn more about the Defibtech Pediatric Training Pad Package (5 Sets) do not hesitate to get in touch with a member of the team. Just call 800 989 7768 and a member of the team will be happy to assist you.

 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.