Physio Control QUIK-COMBO Training Electrodes (2 P/R)

Physio Control QUIK-COMBO Training Electrodes (2 P/R)

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Physio Control QUIK-COMBO Training Electrodes (2 P/R)

Product Code 11103-000001

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What's Included?

  • 2 pairs of AED Trainer new style training electrodes

Designed for use by an array of Physio Control AEDs, including the LIFEPAK 500 and LIFEPAK 1000, these new style AED training electrode pads will allow you to provide a realistic, hands-on training experience for your students. 

Whether your learners work in an office or in a school, training electrode pads will allow you to demonstrate how an AED would react in a real-life emergency, providing them with the understanding of how to act with confidence if someone around them were to fall victim to sudden cardiac arrest.

Unlike their medical counterparts, training electrode pads can be used multiple times, providing you with a cost-effective solution for your training needs.

About Physio Control

Launched in 1955 by Dr. Karl William Edmark, Physio Control has become one of the world’s most well-known AED manufacturers and distributors.

Physio Control envisions a world where no person dies as a result of a treatable medical condition. This goal has led them to develop some of the world’s most recognisable AEDs, including the Lifepak CR2.

More Information

Got a question about this product? Our Advisors are always on hand to help.

Simply call 888 820 0760 and one of our advisors will be happy to answer your questions. 

 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.