Physio Control LIFEPAK CR2 Wall Bracket - White/Red

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Physio Control LIFEPAK CR2 Wall Bracket - White/Red

Product Code 11210-000046USA

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What's Included?

  • LIFEPAK CR2 Wall Bracket

For use with the LIFEPAK CR2 from Physio Control, this Wall Bracket will store your AED in a way that is safe and secure, but easily retrievable in the event of an emergency.

This wall bracket has been designed to be used with the LIFEPAK CR2 AED and offers a simple, cost-effective storage option that takes up little space. The design of the bracket is accompanied by the universal symbol for AEDs, so bystanders and visitors to your premises know the bracket contains a life-saving AED.

Knowing where your closest life-saving device is located can help to save vital time during a cardiac emergency. When someone has fallen victim to sudden cardiac arrest, every second counts and it is essential that the definitive treatment is delivered as swiftly as possible as this provides the casualty with the highest chance of survival.

How to Use

Simply hang the wall bracket in a central indoor location and you're all set. Ensuring your AED is easily accessible and highly visible will ensure prompt treatment is given in an emergency situation.

More Information

Got a question regarding the LIFEPAK CR2 Wall Bracket or any of our other products? Just get in touch by calling 888 820 0760 and a member of the defibshop team will be happy to assist you with any questions or queries you may 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.