Pediatric AED Trainer QUIK-COMBO training electrodes

Pediatric-AED-Trainer-QUIK-COMBO-training-electrodes

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Pediatric AED Trainer QUIK-COMBO training electrodes

Product Code 11250-000045

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What's Included?

  • 1 set of Pediatric AED Trainer QUIK-COMBO training electrodes 

Designed for use with the Physio Control Lifepak CR Plus Training Unit, the Pediatric Training Electrodes will allow learners which work in environments frequented by children to have hands-on training using what they would use in a real-life cardiac emergency. 

These pediatric training pads will allow for a realistic, hands-on training experience, using the same equipment that would be used in a real-life emergency. Unlike their clinical counterparts, these can be used multiple times, providing you with a cost-effective solution for your training.

The training electrode pads allow the students to practice the correct positioning of the pads to ensure the most effective defibrillation can be delivered to a child. Once placed on the training manikin, the pads will then activate the stage of the training experience. The training then simulates the analysis of the patient and determines whether the patient requires shock therapy. This process allows students to learn and understand what would be required of them in a real emergency.

About the Manufacturer

For over five decades, Physio Control has been providing medical professionals and the general public with life-saving AEDs.

They are continually aiming to the goal of a society in which no one dies from cardiac arrest, a condition that could have been treated.

More Information

Got a question about the Pediatric AED Trainer QUIK-COMBO Training Electrodes? The defibshop team are happy to help.

To get in contact with one our friendly advisors, 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.