Physio Control Lifepak 1000 Battery Replacement Kit

Physio Control Lifepak 1000 Battery Replacement Kit

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  • lifepak-1000-for-use

Physio Control Lifepak 1000 Battery Replacement Kit

Product Code 11141-000100USA

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What's Included?

  • Lifepak 1000 Battery Kit

For use with the Lifepak 1000 AED range, this robust piece of equipment will provide you with a replacement battery for your Lifepak 1000 AED, ensuring it is fully charged and ready for use in a rescue.  


  • 5-year battery life

How to Use

Symbols on the AED’s screen will appear that determine whether the device is ready for use or if it requires attention. If the readiness indicator in the top right corner of the device shows “OK” the device is ready for use. If the battery bar is only showing one power bar that is flashing, this means it is time to replace the battery.

Simply install the battery into the corresponding compartment on the AED and you’re all set!

About the Manufacturer

Physio Control is one of the world’s leading manufacturers of AEDs.

Since their launch in 1955, they have gone on to develop, innovate and improve their AED range with the vision of creating a society in which no one dies at the hands of a treatable medical condition – cardiac arrest.

More Information

Do you require further information about the Lifepak 1000 replacement battery or any of the other products listed on our website?

The defibshop team will be happy to assist you with any questions or queries you may have. Get in touch with one of our friendly advisors on 888 820 0760.


 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.