AED Awareness Placard, red


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  • AED-Awareness-Placard-Red

AED Awareness Placard, red

Product Code 989803170901

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What's Included?

  • AED Awareness Placard, red

After someone falls victim to sudden cardiac arrest, it is essential they receive the definitive treatment as quickly as possible. This placard ensures that both trained and untrained responders are confident in delivering the treatment to the patient.

If a victim of sudden cardiac arrest receives the definitive treatment within 3-5 minutes of collapsing, their survival chance significantly increases from 6% to 74%. This is one of the many statistics that prove why it is essential to have a readily available AED onsite.

This placard provides the responder with a graphic step-by-step guide, so regardless of the users training level they can confidently deliver the required treatment to the victim of sudden cardiac arrest.

About the Manufacturer

Over time, Philips has become of the world's leading AED manufacturers. Whether you require an AED for your workplace, school or your local area, Philips has an AED to suit your needs.

Quick and effective, Philips life-saving devices provide the responder with comprehensive audio instructions, so the user feels fully informed during the rescue.

More Information

If you would like to learn more about the AED Awareness Placard, red, the defibshop team are here to help.

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