Philips OnSite and HS Pediatric Training Pads


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  • Pediatric-Training-Pads-OnSite-and-HS-trainer

Philips OnSite and HS Pediatric Training Pads

Product Code M5074AUSA

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In Stock

What's Included?

  • 1 set of Pediatric OnSite and HS training electrode pads

These Pediatric Training Pads are for use with your OnSite and HS training unit and will help you to create the most realistic cardiac rescue training experience for potential users who work within a child-based environment.

Designed to replicate clinical electrode pads, these pediatric Training Pads come equipped with helpful visual instructions, allowing learners to practice placing electrodes effectively on a child patient, who will require different treatment to an adult.

Why do I need Training Pads?

Prior training can help users become more confident with the operation of an AED, giving them a deeper understanding of the process, how to follow the unit’s instructions, apply electrodes and when to deliver CPR. Putting these life-saving steps into practice will help to fully prepare responders for a range of scenarios so they can have confidence in the treatment they provide in an emergency.

Unlike clinical pads, training pads can be used multiple times for training purposes, allowing learners to become comfortable with the pad application and what to expect throughout the process.

More Information

Got a question for one of our advisors? The defibshop team are only a phone call away! To get in touch, simply call 800 989 7768 where a member of our team will answer any queries you may have. 

 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.