Philips FR3 Training Pack


Additional Images

  • FR3-Training-Pack

Philips FR3 Training Pack

Product Code 989803150191USA

0 reviews

In Stock

What's Included?

  • FR3 Training pack

To complement your FR3 Training Unit, this optional accessories pack will enhance a learners training experience when getting hands on with a training AED unit. 

Providing an additional 3 simulation scenarios, this kit helps to widen a user’s experience; helping potential responders to become more confident when operating their clinical FR3 AED. These additional simulations will help users become more comfortable with the potential scenarios they might be faced with when treating a victim of cardiac arrest, allowing for a more efficient rescue.

How to Use

With a separate set of training electrodes, a training battery and more to complement your FR3 training AED, you can set up your unit as though a real clinical AED to allow users to become more hands-on with the device, in a safe and calm environment.

Insert the battery, attach the pads and away you go! Your AED will go through the stages of the rescue process as though real treatment is taking place, allowing users to become familiar with the chain of survival and understanding how to handle each scenario as it occurs.

 More Information

Want to learn more about the FR3 Training Pack? Our helpful advisors are only a phone call away. To get in touch, call 800 989 7768 and a member of our team will help you any way they can.


 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.