Cardiac Science Powerheart G3 AED IntelliSense Lithium Battery 9300E Model


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Cardiac Science Powerheart G3 AED IntelliSense Lithium Battery 9300E Model

Product Code 9146-301

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What's Included?

  • Powerheart G3 AED IntelliSense Lithium Battery 9300E Model

An AED’s battery is what provides the device with the power to deliver a potentially life-saving shock in a cardiac emergency. 

Ensuring your AED has a fully charged battery and is completely operational will provide you with the peace of mind that it is ready to use at a moment’s notice.

A fully operational battery will also allow your AED to perform the required maintenance programs, ensuring each and every part of your device is functional and in a rescue ready condition.

Key Features

  • Designed for use with Cardiac Science’s Powerheart G3 AED range
  • 4-year performance guarantee
  • Ensures your AED is always in a rescue ready condition

How to Use

When an AED’s battery needs replacing, you will receive either an audio notification in the form of a beeping noise, or you could even receive an email alerting you that your battery is about to expire. Replacing your Powerheart G3’s battery couldn’t be simpler.

Simply remove the currently installed battery and then insert your new battery into the slot and you’re all set. The AED will always use the battery power in the background whilst carrying out the required self-maintenance checks which help ensure the electrode pads, hardware, and software of the AED are all functional and ready for use if an emergency arose.

About Cardiac Science

Since their launch back in 1991, Cardiac Science has gone on to be one of the world’s leading AED manufacturers with professional grade technology at the heart of each and every one of their AEDs.

All Cardiac Science AEDs have been designed with simplicity and ease of use in mind, so whether you’re a trained professional or a first-time responder, you can feel confident in the treatment you’re providing to the victim of sudden cardiac arrest.

More Information

If you require any further information about the Powerheart G3 AED IntelliSense Lithium Battery 9300E Model, the defibshop team are the ones with all the answers.

To speak to one of our friendly advisors, call 0000 000000 and they’ll be happy to help you in any way they can.


 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.