Defibtech Lifeline Training Pads (5 pack)

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Defibtech Lifeline Training Pads (5 pack)

Product Code DDP-105TRUSA

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What's Included?

  • 5 pack of Lifeline Training Pads

Enhance your training experience with the Lifeline Training Electrode Pads. When preparing for an emergency rescue, you want to ensure training prior to a cardiac event is as realistic and beneficial as possible, to build confidence and increase chances of survival. 

This pack of 5 Training pads ensures you’re able to replace used electrodes so you can continue to deliver accurate training scenarios for your students.

Enhancing the Training Experience

Specifically designed for use with Lifeline training AEDs, these training electrodes allow you to deliver effective and true-to-life training time and time again by replacing the electrodes, once they become compromised or overly worn.

By providing hands-on and realistic training, you can help to create prompt and confident first aiders. In the event of a cardiac emergency, you want to be sure your students will have the knowledge and ability to provide the vital care to help save a life.

Understanding accurate electrode pad placement is essential for defibrillation. These pads allow you to cover this part of training as many times as needed until your students are comfortable with the rescue steps which follow a cardiac arrest.

More Information

Got a question about the Lifeline Training Pads? The defibshop team can answer any questions you may have. To get in touch, simply call 888 820 0760 where one of our advisors will gladly answer any queries you may have.

 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.