Philips HeartStart AED Trainer 2
Philips HeartStart AED Trainer 2
Product Code M3752A
- AED Training Unit
- Carrying Case
- 1 set of AED Training Pads
The Philips HeartStart AED Trainer 2 will allow users to demonstrate a realistic training experience for potential responders as they learn to operate the medical device.
AED Training Units simulate multiple cardiac scenarios to help learners understand the potential outcomes they may have to deal with when caring for a victim of cardiac arrest.
- Philips HeartStart AED Trainer 2
- Adult-size reusable training pads - 1 set
- Quick reference instruction card
- User guide
- Carrying case
As the Philips is designed to look and operate just like its clinical counterpart, without the shock delivery; learners can build their knowledge with a hands-on training experience. While all AEDs are designed to be intuitive and easy to use, prior training can help to create fast and effective users who are confident in the treatment they apply.
The trainer is designed to send out voice prompts in several languages and helps in selecting a pre-configured training scenario out of the given 10 scenarios. Featuring advanced technology, the trainer promotes realistic response to electrode placement on the manikin.
The trainer includes 10 realistic training scenarios, pre-configured into the Trainer so responders can react to every potential outcome during the rescue.
You can learn more about this product simply by contacting the defibshop AED Product Specialist team, call 800 989 7768 to speak with us directly.
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.