Philips OnSite Replacement Pediatric Pads


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  • Replacement-Pediatric-training-Pads

Philips OnSite Replacement Pediatric Pads

Product Code M5094AUSA

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What's Included?

  • Replacement Pediatric Training Pads

These replacement Pediatric Training Pads are for use with your OnSite Training Unit and will allow learners to practice realistic training scenarios, helping them to build confidence for treating a child suffering a cardiac arrest.

Prior training will help potential users understand every step of the rescue process and will increase their confidence in applying treatment to a child, who requires slightly different treatment when being treated for cardiac arrest.

Effective pad placement is essential in a rescue, which is why training electrodes are beneficial for helping users to get comfortable with placing them correctly for optimum defibrillation.

While Pediatric training pads can be used multiple times, should your original pair become worn or broken, we advise a replacement pack to ensure your training is as realistic and beneficial for the learner as possible. The pads have a sticky adhesive just like their clinical counterparts and can be used to practice pad placement on your training manikin.

More Information

Need some advice on which products best suit your training needs? Our helpful defibshop team are only a phone call away. To get in touch, simply call 800 989 7768 where one of our advisors will assist in helping you find the perfect products for 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.