ZOLL Trainer Electrode, pedi padz II (6 pairs per case)

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ZOLL Trainer Electrode, pedi padz II (6 pairs per case)

Product Code 8900-000861-01USA

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What's Included?

  • Trainer Electrode, pedi padz II (6 pairs per case)

These Trainer Electrode Pedi Padz are for use with ZOLL Training Units and will allow users to understand effective pad placement for pediatric patients.

Separate algorithms are used to analyze an adult and child’s heart during a cardiac rescue. AED units can defibrillate children up to the ages of 8 years old using Pedi-Padz; once the electrode pads are connected to the AED, the joule level automatically reduces to a level which is safe for a child.

How to Use

These Trainer Electrodes will help users to understand exactly where to place electrode pads on a child for effective defibrillation.

Care for a child in cardiac arrest differs to that of an adult, which is why we recommend training prior to use, to give responders a better understanding of how to operate a unit, and what changes to make to the rescue process when providing treatment to a child.

These pads, when connected to the trainer can be used multiple times to help increase the confidence of users. Please note that unlike clinical pads, these training Pedi Padz will not provide a shock and are purely for re-enactment purposes.

More Information

Got a question about this product? Our helpful team of Product Specialists are here to help.

To get in touch, call 800 989 7768. 

 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.