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

AED-Trainer-QUIK-COMBO-training-electrodes-2-P/R

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  • AED-Trainer-QUIK-COMBO-training-electrodes-2-P/R

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

For use with the AED trainer unit, this product provides you with QUIK-COMBO training electrodes to help you provide the most hands-on and realistic training experience as possible. 

This set of QUIK-COMBO training electrodes will ensure your learners are able to fully practice and understand the rescue process required in a cardiac arrest situation with hands-on and realistic training. These pads, unlike their medical equivalents, are reusable and are designed to be used on CPR manikins only.

These pads teach the learners where the electrode pads should be placed on a casualty for the most effective defibrillation so they can be applied swiftly, should a real cardiac emergency occur.

Once the pads have been placed on the training manikin, the training unit will then run through the treatment simulation, giving students a realistic approach to their training experience.

About the Manufacturer

Physio Control has been innovators of life-saving technology since 1955, creating devices that trained and non-trained rescuers can use with confidence.

Their AED range is designed to be user-friendly so that untrained users can react to a cardiac emergency with confidence and feel assured in the treatment they’re delivering.

More Information

Got a question for us? The defibshop team are happy to answer any questions you may have regarding any of the products on our site.

Your satisfaction is our number one priority; to get in contact with one of our friendly advisors and find the right products for your needs and budget, simply 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.