Physio Control Lifepak 12 REDI-CHARGE Adapter Tray

Physio Control Lifepak 12 REDI-CHARGE Adapter Tray

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Physio Control Lifepak 12 REDI-CHARGE Adapter Tray

Product Code 11141-000116

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What's Included?

  • LIFEPAK 12 REDI-CHARGE Adapter Tray

Designed for use with Physio Control’s REDI-CHARGE battery charger, this adapter tray allows you to charge two batteries to power your LIFEPAK 12. 

Ensuring your LIFEPAK 12 AED/ Monitor is ready for use and has a full battery will allow the device to be used in a rescue. Without a charged battery, the AED/ Monitor will not be able to deliver a shock to the patient, should one be required. Also, the device will not be able to perform the required maintenance checks which help ensure the AED is in a full working order.

**Please note: this adapter tray is designed to be used for charging the LIFEPAK 12 Lithium-Ion batteries only***

About the Manufacturer

Since their launch in 1955, Physio Control has gone on to become one of the world’s leading and most renowned AED designers and manufacturers.

Each and every device, created by Physio Control has been designed with simplicity and ease of use in mind. This allows medical professionals and untrained responders alike, to respond to a cardiac emergency with confidence.

More Information

If you would like more information about the LIFEPAK 12 REDI-CHARGE Adapter Tray, the defibshop team are always on hand to help.

To speak to one of our specialists, simply call 800 989 7768 and they will be happy to share their knowledge about this product with 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.