AED Wall Cabinet with alarm - surface mount, rolled edges

AED Wall Cabinet with alarm - surface mount, rolled edges

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AED Wall Cabinet with alarm - surface mount, rolled edges

Product Code 11220-000079USA

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What's Included?

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

Storing your AED in a cabinet is advisable to help increase the visibility of your life-saving AED. In the event of an SCA, quick action, CPR and defibrillation are the only definitive treatment for an increased chance of survival. 

This wall cabinet is designed by Physio Control and will help you to increase awareness of your device in any indoor location. Easily mounted to the wall, you can ensure your AED unit is kept at eye-level, so it is easily locatable in the event of an emergency.

Effective Storage

Not only will keeping your AED in a wall cabinet highlight your AED, but will protect it from common environmental factors such as dust which can potentially harm your device if it meets the software.

Keeping your AED safely stored will ensure it can provide the most effective defibrillation possible when you need it most.

 More information

Want to learn more about the AED Wall Cabinets from Physio Control? You can get in touch with the defibshop AED Product specialists by calling 0000 00000.

With many years in the AED industry under our belt, you can have confidence that we can provide you with honest and impartial advice to help you find the perfect product for 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.