Physio Control LIFEPAK 500T Replacement simulated battery pack
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Physio Control LIFEPAK 500T Replacement simulated battery pack
Product Code 11250-000006
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What's Included?
- LIFEPAK 500T Replacement simulated battery pack
This replacement battery pack is for use with the Lifepak 500 AED Training System and is required when the original simulated battery pack requires replacement.
The pack requires 4 “D” cell batteries to function to help you provide an effective training experience.
Effective Training for Effective Responders
Whilst all AED is designed to be easy to use by everyone, additional training can help to increase user confidence, helping responders to understand the rescue steps, practice their CPR skills and know what to expect during a real-life rescue.
By choosing to have a training system unit which replicates your clinical AED, potential-users can get to grips with the unique features and functions and familiarize themselves with how to operate the unit, helping to achieve a more effective and efficient rescue in the event of a cardiac emergency.
More information
Need some assistance in finding the right product to suit your existing equipment? The AED Product Specialists are on hand to take your call. To get in touch, dial 800 989 7768 during our opening hours where a member of our team will happily assist you with your inquiry.
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.