AED Wall Sign Traditional w/logo, Tent, 7x8


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AED Wall Sign Traditional w/logo, Tent, 7x8

Product Code 11998-000332

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What's Included?

  • AED Wall Sign Traditional w/logo, Tent, 7x8

After purchasing your life-saving AED, it is important that you ensure it is visible. The AED Wall Sign Traditional w/logo, Tent, 7x8 will ensure that your device is visible and highlighted from a variety of angles and that bystanders don’t mistake the signage for anything other than an AED. 

The 3D design of this wall sign will ensure bystanders at all angles in your location are notified and know where the AED is located, so should an emergency arise, the AED can be accessed quickly, and the device delivered to the victim as quickly as possible.

For every minute that the victim of cardiac arrest does not receive the required treatment, their survival chance drops 10%. Ensuring that the device is delivered to the scene and the treatment is administered as swiftly as possible will help to provide the highest chance of survival.

About Physio Control

Physio Control launched back in 1955 and has envisioned a society in which no one person dies as a result of a treatable cardiac event.

This vision has led them on to continually develop their Lifepak AED range and become one of the world’s most recognized AED developers and manufacturers.

Each and every AED created by Physio Control caters for all levels of training, so whether you’re a medical professional and have rescued someone before or you’re a first-time responder and have never used an AED, you can feel confident in the treatment you’re delivering to the patient.

More Information

If you require more information about the AED Wall Sign Traditional w/logo, Tent, 7x8 speak to the defibshop team!

To speak to one of our friendly, expert advisors, call 888 820 0760 and they’ll be happy to help in any way they can. 

 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.