Wall Mount Bracket for Lifepak 1000 and Lifepak 500

wall-mount-lifepak-1000

Additional Images

  • wall-mount-lifepak-1000

Wall Mount Bracket for Lifepak 1000 and Lifepak 500

Product Code 11210-000001USA

0 reviews

In Stock

What's Included?

  • Wall mount bracket

Designed for use with Physio Control’s Lifepak 1000 and Lifepak 500 AEDs, this wall mount bracket ensures that your AED is safe, secure and easy to retrieve in the event of an emergency. 

The Wall Mount Bracket for the Lifepak 1000 and Lifepak 500 ensures that your AED is highly visible to everyone in the area whilst being well protected and easily retrievable so the AED can be delivered to the scene of the emergency swiftly, closing the gap time between the victim collapsing and defibrillation.

How to Use

Hang your Wall Mount Bracket indoors in a central, accessible location for bystanders and staff members. Having the device visible will help both bystanders and staff familiarise themselves with the AEDs location so that if someone did fall victim to cardiac arrest, they would know where the AED was located, allowing for swift retrieval and treatment.

The built-in strap provides your AED with extra security, ensuring that it is safe and secure whilst still on display. 

More Information

If you would like to learn more about the Wall Mount Bracket for the Lifepak 1000 and Lifepak 500 AEDs, feel free to get in touch with one of our friendly advisors.

Our friendly and knowledgeable advisors are the ones with all the answers to your questions. They can be contacted directly on 888 820 0760.

 

 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.