Physio Control Lifepak 15 AC Power Adapter

Physio Control Lifepak 15 AC Power Adapter

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Physio Control Lifepak 15 AC Power Adapter

Product Code 11140-000072USA

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What's Included?

  • 1 Lifepak 15 AC Power Adapter

Designed for use with Physio Control’s Lifepak 15 AED range, this AC Mains Power Cable will keep your AED battery sufficiently charged to make sure your AED is in a state of readiness at all times.

This AC Mains Power Cable is to be used with your Lifepak 15 AED. It will help ensure that your device is ready to be used at a moment’s notice by charging the battery to a sufficient level.

About the Manufacturer

With AEDs manufactured and designed to fit rescuers of all abilities, Physio Control ensures that whether you’re a medical professional or a first-time responder, you can effectively save the life of a cardiac arrest victim with one of their AED devices.

Since their launch in 1955, they have been a world leader in the manufacturing of life-saving AED equipment. Their Lifepak 1000 device was selected by NASA to travel into space and take residence on the International Space Station; this was an amazing achievement for the company.

More Information

If you would like to learn more about the Lifepak 15 AC Mains Power Cable, then we invite you to get in touch with the defibshop team.

We pride ourselves on providing expert, impartial advice to help you find the perfect products for your budget and requirements. To get in touch, simply call 800 989 7768.

 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.