Defibtech Lifeline AED Trainer Package
Defibtech Lifeline AED Trainer Package
Product Code DCF-A350T-EN
- Defibtech Lifeline Trainer AED
- Training Battery (rechargeable)
- Training Battery Charger
- Adult Training Pads
- Remote Control
Ready to get to know your Defibtech Lifeline AED device? This Standalone Trainer AED Package will allow you to get hands on with your unit, so you can explore an exact replica of your functioning AED in the safety of a training environment.
This package will equip you with a training model of the Defibtech Lifeline AED alongside the essential accessories to allow you to replicate rescue scenarios. This will help you get better acquainted with the unique features of your device, boosting user confidence should you need to use it in the event of a cardiac emergency.
Should a cardiac arrest occur, CPR and defibrillation must be delivered promptly to help boost chances of survival. Getting to know your AED can help to increase confidence, so you’re fully aware of its functions and what to expect when using it in an emergency.
As this package comes inclusive of reusable battery and electrode pads, you can use this training package time and time again to create realistic training scenarios to boost the confidence of all potential users and refresh their rescue skills.
Want to learn more about the Standalone Trainer AED Package? The defibshop AED Specialists are here to take your call. You can get in touch by calling 800 989 7768 where a member of our team will help 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.