AED Wall Cabinet with alarm and strobe - surface mount, rolled edges

AED Wall Cabinet with alarm and strobe - surface mount, rolled edges

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AED Wall Cabinet with alarm and strobe - surface mount, rolled edges

Product Code 11220-000084

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What's Included?

  • AED Wall Cabinet with alarm and strobe - surface mount, rolled edges

Designed for use with a variety of Physio Control's life-saving devices, the AED Wall Cabinet with alarm and strobe is the perfect way to ensure your AED is kept safe and secure, prior to use.

Compatable with the LIFEPAK 500, LIFEPAK 1000, LIFEPAK CR Plus and LIFEPAK EXPRESS, this wall cabinet will provide your life-saving device with the utmost protection so you can have peace of mind that your AED is safe, secure and in a ready-to-use condition.

This cabinet has been manufactured with both an alarm and a strobe light which will both be deployed when the cabinet's door is opened. These extra security features will alert others in the area to the cardiac emergency and prompt further assistance during the rescue. The cabinet is also equipped with a transparent window so you can see your AED situated inside and help raise awareness of the cabinet's contents.

About the Manufacturer

For over half a century, Physio Control have been producing life-saving devices and technologies to assist both medical professionals and the general public in treating cardiac arrest.

They continually are researching and innovating to create new technologies that can help to save more lives.

More Information

If you would like to learn more about the AED Wall Cabinet with alarm and strobe - surface mount, rolled edges, get in touch with the team here at defibshop.

Get in touch by calling 888 820 0760 and one of our experts will be happy help.

 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.