Physio-Control LIFEPAK 500 AED Training Electrode Set

Physio-Control LIFEPAK 500 AED Training Electrode Set

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Physio-Control LIFEPAK 500 AED Training Electrode Set

Product Code 11101-000004USA

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What's Included?

  • 5 sets of Physio-Control LIFEPAK 500 AED Training Electrodes

Designed for use with Physio Control’s LIFEPAK 500 AED trainer unit, these electrode pads will allow your learners to thoroughly understand how to react to a real life cardiac arrest emergency. 

The LIFEPAK 500 AED training electrode pads provides you with 5 sets of training electrode pads which can be used to teach learners how to use this specific activity in an emergency situation. Once placed on the training manikin, the electrodes will activate the next step of the rescue process on the AED, displaying to the learners exactly how the LIFEPAK 500 would react in a real rescue.

These pads are exactly the same as their medical counterpart, however, unlike the clinical grade electrodes, these can be used multiple times, providing you with a cost-effective solution to training your learners.

About the Manufacturer

Physio Control has been around since 1955 and has become one of the world’s most well-known AED manufacturers.

Their ultimate goal is to create a world where no one dies as a result of a treatable medical condition. This goal has led them on to develop the Lifepak CR+, one of the most well-known AEDs on the market that allows learners of all training levels to respond with confidence to a medical emergency.

More Information

If you require further information about Physio Control’s LIFEPAK 500 AED Training Electrodes, the defibshop team are always on hand to help.

Call 888 820 0760 to speak to one of our advisors who’ll 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.