Early Defibrillation - Training & Implementation Guide

Early Defibrillation - Training & Implementation Guide

Product Code 26500-000181USA

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What's Included?

  • 1 Training and implementation guide

Designed by Physio Control, this Training and Implementation Guide will tell you everything you need to know about Early Defibrillation. 

This guide outlines the importance of early defibrillation and the impact it can have on the casualty’s chance of survival and recovery. For every minute that passes without treatment, the casualty loses 7-10% of their survival chance, so the sooner treatment is delivered, the better.

This is also a perfect tool to support training as it can broaden learner’s knowledge of how AEDs function and save lives. Once learners have broadened their knowledge on the science of AEDs they will feel more confident using the device during a cardiac emergency.

About the Manufacturer

Since 1955 when Physio Control was first established, over the years they have continued to grow into a successful market leader in the development and manufacturing of life-saving equipment.

The user-friendly features on their devices, audio prompts, and easy-to-understand diagrams, almost anyone can use the Physio Control AED range.

More Information

If you’re looking for more information about the Early Defibrillation Training and Implementation Guide or any other product listed on our website, then the customer service team are on hand to help.

Contact one of our friendly advisors on 888 820 0760. 

 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.