Physio Control Wall Cabinet - Fully-recessed for AED, 1.5" Trim

Wall-Cabinet-Fully-recessed-for-AED-1.5-Trim

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Physio Control Wall Cabinet - Fully-recessed for AED, 1.5" Trim

Product Code 11998-000293

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What's Included?

  • Wall cabinet 

This Flat Trim Wall Cabinet provides you with an effective storage solution for your LIFEPAK 500, LIFEPAK 1000, LIFEPAK CR Plus, or LIFEPAK EXPRESS AED, ensuring it is visible and accessible in the event of a cardiac emergency.  

Designed to be a sleek and smooth addition to the walls of your workplace, this cabinet is manufactured in steel with a baked on white epoxy finish. The built-in alarm will help to deter thieves and will help to alert those nearby when a rescue is taking place; this feature can be easily armed or disarmed using the key lock.

With each cabinet order, you’ll receive an eye-catching AED Wall Placard and CPR/AED wall poster to help increase visibility to your unit.

Compatible with LIFEPAK 500, LIFEPAK 1000, LIFEPAK CR Plus, or LIFEPAK EXPRESS AEDs.

How to Use

Install your cabinet in an accessible and visible location so bystanders can easily retrieve it, should someone suffer a cardiac arrest.

Its robust design will provide additional protection to your AED if kept outdoors, shielding it from harsh environmental factors, ensuring it is safe and secure at all times.

More Information

Want to learn more about the Fully Recessed Wall Cabinet? Whether you have a question about this product or any of the other storage options on our website, our helpful defibshop team are on hand to help.

To get in touch, simply call 888 820 0760, where an advisor will assist you with any queries you have. 

 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.