Philips AED Trainer 3
Philips AED Trainer 3
Product Code 198-00650
- Quick Start Guide
- 4 x AA Batteries
- Infant/Child Key with tether
- Operating System Card
- Philips Training Pads III
- Philips Interconnect cable
- External Manikin Adapter
Designed to emulate the Heartstart FR3 AED range, the AED Trainer 3, Trainer only from Laerdal will ensure your students are equipped with the knowledge of how to react and respond with confidence during a cardiac emergency.
This AED training unit provides trainees with the opportunity to have first-hand experience with the Heartstart FR3's unique functions during a training situation.
Emulating its clinical counterparts functions, appearance and operation will ensure confidence during a real-life emergency as your students will know what is required of them for a successful rescue.
How to Use
The AED Trainer 3, Trainer only is capable of simulating the different stages of the rescue process, providing learners with an insight as to how the clinical unit would function in a real-life emergency.
The AED Trainer 3, Trainer only provides learners with the ultimate preparation tool for learning how to treat someone who has suffered a cardiac arrest.
About the Manufacturer
Laerdal's beginnings were in a small publishing house that specialized in children's books and greetings cards. Soon after they started to develop children's toys which led to them developing first aid manikins.
Fast forward to the present day and Laerdal are one of the world's most recognized medical equipment manufacturers. Their training manikins are the choice of medical professionals around the world and they've helped train over 400 million people in essential life-skills.
If you would like more information about AED Trainer 3, Trainer only the defibshop team are here to help.
To speak to one of our advisors, call 800 989 7768 and they'll be happy to assist you in 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.