ZOLL AED Plus/Pro Pediatric Pedi Padz II - Single


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ZOLL AED Plus/Pro Pediatric Pedi Padz II - Single

Product Code 8900-0810-01USA

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In Stock

What's Included?

  • 1 set of Pediatric Pedi Padz

Keeping a pair of pediatric pads with your ZOLL AED will allow you to deliver a rescue to a victim of cardiac arrest, no matter what their age.

Sadly, cardiac arrest can occur in anyone of any age, which is why manufacturers have developed specific pediatric electrode pads which will automatically reduce the shock level to one which is safe for a child between the ages of 1-8 years old.

Once connected to your ZOLL AED, the usual 150-joule shock is reduced automatically to a safe level through the electrode pads, all you have to do is connect them as you would regular pads and begin the rescue.

Pad Features:

  • For use on children aged 1 – 8 years old.
  • Pediatric pads administer lower levels of energy to protect children from harm
  • Preconnected electrodes to save valuable seconds
  • Clear and simple diagrams
  • Long-lasting pads that expire after 18-24 months.

How to Use

Remove the pads from the packaging following the visual prompts on the packet. Place on the child’s bare chest and in the centre of the back as indicated in the directions. The AED will then analyse the child’s heart rhythm and will deliver a shock with lower levels of energy than adult pads if needed.

More Information

Want to learn more about the ZOLL Pediatric Pedi Padz? Our knowledgeable defibshop advisors are the ones to call.

Dial 800 989 7768 and you’ll be connected with defibshop direct.


 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.