Cardiac Science Powerheart Non Rechargeable Intellisense Lithium Battery 9145


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Cardiac Science Powerheart Non Rechargeable Intellisense Lithium Battery 9145

Product Code 9145-301

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What's Included?

  • Powerheart G3 Pro AED IntelliSense Lithium Battery (9300P model)

Designed for use with the Powerheart G3 Pro AED range, this non-rechargeable Intellisense Lithium Battery will keep your AED in a state of readiness so it’s always able to deliver a shock to a victim of cardiac arrest.

Ensuring your AED’s battery is fully charged is essential for the device to deliver a potentially life-saving shock after someone has fallen victim to sudden cardiac arrest.

A full battery in an AED will help to ensure that your device is always ready to deliver a life-saving shock whenever needed. The self-checks carried out by the AED also require battery power; this helps to ensure your device is in good working order.

Battery features

  • Specifically designed for use with the Powerheart G3 Pro
  • Helps to ensure the AED is operational and ready for use at the moment’s notice
  • 1-year guarantee

How to use

When your AED’s battery is coming to the end of its life and needs replacing, a beeping notification will alert you. Installing a new battery couldn’t be simpler; simply take out the old battery and insert the new one and your device is ready for use. A charged battery will also enable your device to carry out vital maintenance checks whilst you’re not using the device. These help to ensure your device is still in a rescue-ready condition.

The AED will use the battery power in the background at all times when the unit inspects and maintains the hardware, software, electrode pads and other systems so that in the event of a cardiac emergency, the device can be used.

More Information

If you would like to learn more about the Cardiac Science Non-Rechargeable IntelliSense Lithium Battery 9300P, the defibshop team are the ones with all the answers.

Call one of our advisors on 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.