Cardiac Science Powerheart G3 AED IntelliSense Lithium Battery - TSOC142A Certified


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Cardiac Science Powerheart G3 AED IntelliSense Lithium Battery - TSOC142A Certified

Product Code 9147-201-TSO

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What's Included?

  • Powerheart G3 AED IntelliSense Lithium Battery

The Powerheart G3 AED IntelliSense lithium battery is essential for ensuring your AED is operational and rescue ready at all times. Designed for use with the Powerheart G3 & G3 Plus AED, this battery is non-rechargeable. 

Ensuring your AED has a full battery is crucial for the live-saving device and its ability to administer the life-saving shock needed to treat a victim of a cardiac arrest.


  • Designed especially for use with the Powerheart G3 and G3 Plus defibrillators
  • Ensures that the defibrillator is rescue-ready at all times
  • 4-year unconditional warranty

How to use

When you are notified and become aware that the current battery in your AED needs replacing from a reminder email or the AED itself confirming the expiration of the battery, it is simple to add a new one. This will ensure your device is fully functional all times in the case of a cardiac emergency.

About Cardiac Science

Cardiac Science is a global leader when it comes to the development and manufacturing of AEDs. Their expertise in AEDs and accessories have resulted in some of the most popular units on the market. Their innovation has allowed them to provide life-saving devices which help rescuers deliver effective care as efficiently and quickly as possible.

More Information

If you would like to find out more about the Powerheart G3 AED IntelliSense Lithium Battery or any of our other products, the defibshop team are on hand and would be more than happy to answer any questions or queries you may have. You can contact the defibshop team directly 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.