Physio Control Lifepak 1000 Training Unit
Physio Control Lifepak 1000 Training Unit
Product Code 99996-000117
- Lifepak 1000 training unit
Want to boost user confidence in the operation of a clinical AED? The Lifepak 1000 Training Unit is the perfect training tool to help you increase your knowledge of the unique features and functions of your real-life unit.
If you’re the proud owner of the Lifepak 1000, you might want to consider purchasing a training version of the AED, to help you get hands-on with your device, so should you have to use the real unit in the event of an emergency, you’re fully confident in how it operates.
This training unit is designed to simulate the functions of a live defibrillator so that learners can get a feel for how the defibrillation process works. They can explore user-friendly features such as the audio step-by-step guides and visual prompts, discovering how easy the device is to use.
How to Use
This training AED has been created to simulate the same functions as your operating AED to provide potential rescuers with a realistic and beneficial experience of how the device works. Users can practice the different stages of the defibrillation process, again and again, to ensure they’re fully confident in every step of the rescue.
From applying the electrode pads accurately, to delivering CPR and pressing the shock button to administer a “shock” the Lifepak 1000 offers potential users the opportunity to familiarize themselves with their AED should a real emergency occur.
If you would like to learn more about the Lifepak 1000 Training Unit or would like to discuss the benefits of AED training, we invite you to call our helpful defibshop team.
As an independent distributor, you can be sure that the advice we provide is completely impartial and tailored to fit your needs; get in touch by calling 800 989 7768.
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.