Defibtech Lifeline Pediatric Electrode Pads for use with View, ECG and PRO


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Defibtech Lifeline Pediatric Electrode Pads for use with View, ECG and PRO

Product Code DDP-2002USA

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What's Included?

  • 1 set of Lifeline Pediatric Electrode Pads for us with View, ECG and PRO

Designed for use with the Defibtech Lifeline View, ECG and PRO AED, the Lifeline Pediatric Electrode Pads are easy to use and reduce the amount of electricity delivered in the shock to a lower level.

These pediatric electrode pads are a vital tool to have if your AED is required to assist a child in cardiac arrest. 

Paediatric pads reduce the joule output from the AED to a level which is suitable for the heart of a child, aged between 1 and 8. The joules are lowered from 150 joules to 50 joules.

Pad features

  • Foil packaging protects the electrodes from being damaged prior to use
  • Pre-connected by design can help save valuable time in a cardiac emergency
  • Designed for usage with the Lifeline View, ECG and PRO AEDs
  • Bold, clear images help the rescuer to apply the pads in the correct position on the patient

Why it matters

Unlike other medical emergencies, children are at just as much risk to suffer a cardiac arrest as an adult. Aspects such as age and gender do not factor for contributing to cardiac arrest.

To save time, the Defibtech Lifeline Pediatric Defibrillation Pads are designed to be pre-connected to the AED in order to assist the swiftly.

The immediate moments after the event are critical. If effective CPR and a life-saving shock from an AED is delivered to the victim within 3-5 minutes of collapse, the survival chances significantly increase from 6% to 74%.

About the Manufacturer

Defibtech is one of the world’s best-known manufacturer, designer and distributor of defibrillators and has been for over 15 years.

They have achieved many awards and accreditations over the years, but possibly their most noteworthy achievement was being the AED of choice to protect the athletes and spectators at the 2006 Winter Olympics in Torino, Italy.

More Information

If you have any questions about the Defibtech Lifeline Pediatric Defibrillation pads, then the friendly defibshop team is here to help.

Simply call 800 989 7768 and one of our knowledgeable team members will be happy to make sure you find the right equipment to suit your needs. 

 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.