Right angle cable (10in) included with ACPA & DCPA

Right angle cable (10in) included with ACPA & DCPA

Product Code 11140-000081

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What's Included?

  • Right angle cable (10in) included with ACPA & DCPA

For use with Physio Control’s Lifepak 15 AED/ Monitor range, the right-angle cable (10in) will allow you to charge your device at a different angle than was originally possible. 

Ensuring your life-saving LIFEPAK 15 device is fully charged will enable you to use it in an emergency situation. A charged battery is required to deliver the potentially life-saving shock to the patient if it is required.

Also, a charged battery will allow the device to carry out the essential self-checks that monitor the AED and its components. This helps to ensure the device is ready for use at a moment’s notice.

About Physio Control

Since their launch in 1955, Physio Control has envisioned a society in which no one person dies as a result of an acute, treatable cardiac event. This has led them on to create some of the world’s most recognized AEDs, notably the LIFEPAK AED range.

Physio Control’s AEDs have been created with ease of use at the heart of the design. This allows both trained and first-time responders to act in a cardiac emergency and feel confident in the treatment they’re delivering to the victim of cardiac arrest.

More Information

If you would like more information about the Right angle cable (10in) included with ACPA & DCPA or any other product on our website, the defibshop team are the ones with all the answers.

Simply call 888 820 0760 and one of our specialists will be happy to answer your questions and queries to the best of their ability.


 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.