AED Sign - Right Arrow

DAC-233-right-arrow

Imagenes Adicionales

  • DAC-233-right-arrow

AED Sign - Right Arrow

Product Code DAC-233

0 reviews

En existencia

What's Included?

  • AED Sign - Right Arrow

Designed to highlight the location of the AED, this Right Arrow sign enables you to direct bystanders and employees alike to the location of your AED in the event of an emergency.

Knowing where your closest AED is located can help save vital time during an emergency. This Right Arrow sign from Defibtech enables you to highlight the location of your life-saving device by simply pointing to where it is kept.

After someone has fallen victim to sudden cardiac arrest, every moment counts and it is of vital importance that the definitive treatment is delivered as swiftly as possible to provide the casualty with the highest chance of survival. Directing bystanders to the location of the AED will allow for a quick retrieval and help to save vital time.

About the Manufacturer

Defibtech have been creating and innovating their Lifeline range of AEDs since 1999. This range of AEDs has been designed to be easy to use, recognizable and portable.

Manufacturerd in the United States, Defibtech now have more than 200,000 in the field and have earned many accolades over the years.

More Information

If you would like to learn more about the AED Sign - Right Arrow, get in touch with our knowledgeable team.

Call 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.