Physio Control LIFEPAK 20 NiMH rechargeable internal battery


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  • LIFEPAK0-20-NiMH-rechargeable-internal-battery

Physio Control LIFEPAK 20 NiMH rechargeable internal battery

Product Code 11141-000068

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What's Included?

  • LIFEPAK 20 NiMH rechargeable internal battery

Designed for use with Physio Control’s LIFEPAK 20 AED range, the NiMH rechargeable internal battery will ensure that your life-saving AED has more than enough power to be used in a potentially life-saving rescue. 

Ensuring your AED has a fully functional battery is an essential part of its maintenance. Without the battery fully charged, the AED cannot provide the potentially life-saving treatment to a victim of sudden cardiac arrest, or perform the required self-tests that ensure its ready for use at a moment’s notice.

About the Manufacturer

Physio Control is one of the world’s leading designers and distributors of AEDs. Simplicity and ease of use is at the heart of every AED and accessory designed by Physio Control, allowing responders of all levels to confidently respond to during a cardiac emergency.

Since their launch in 1955, Physio Control envisions a world in which no one person dies due to a treatable cardiac condition. This vision has led them to design the AEDs that are so well known across the globe.

More Information

If you would like more information about the LIFEPAK 20 NiMH rechargeable internal battery, the defibshop team are here to help.

To speak to one of our advisors, call 800 989 7768 and one of our team members will be happy to assist you.


 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.