Physio Control Lifepak 15 Lithium Ion Battery 5.8 Ah

Physio Control Lifepak 15 Lithium Ion Battery 5.8 Ah

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Physio Control Lifepak 15 Lithium Ion Battery 5.8 Ah

Product Code 21330-001176USA

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What's Included?

  • Lithium Ion Battery 5.8 Ah for Lifepak 15

The Lifepak 15 by Physio Control supports two Lithium Ion batteries with dual battery technology, enabling the user to switch from one power source to the next with ease. The durability of this AED helps the battery to withstand harsher elements, such as impact, high temperatures and humidity. 

How to Use

This battery can be charged when it has already been installed into your AED, by using an AC or DC adapter. The typical charge time is 190 minutes.

To view the current battery levels, take a look at the fuel gauge and/ or the ‘low battery’ message if it is visible. Once the battery power has reached a critically low level, an audio message will sound stating ‘replace battery’ and the device will automatically switch over to the alternative battery.

Users can track the service and remaining service life of your batteries by using the LIFENET data system network.

The power source enables the AED to shock the patient if a shock is required. This shock will be escalating energy, up to a high-energy dose of 360 Joules.

About the Manufacturer

Physio Control aspires for a society in which no dies as the result of a treatable medical condition.

Their technology has been designed with ease of use at the forefront, enabling both medical professionals and untrained users to confidently treat sudden cardiac arrest.

Physio Control has been operating for more than 55 years and has become one of the world’s most well-known manufacturers or life-saving AEDs.

More Information

If you would like any further information about the Lifepak 15’s Lithium Ion Battery, we invite you to call our team of helpful advisors who will gladly assist you with your query.

Simply call 800 989 7768 to get in touch with the team 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.