Physio Control LIFEPAK CR2 Replacement Electrode Kit

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Physio Control LIFEPAK CR2 Replacement Electrode Kit

Product Code 11101-000021USA

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What's Included?

  • Replacement Electrode Kit for LIFEPAK CR2

This replacement Electrode Kit has been designed exclusively for the LIFEPAK CR2, the latest in AED innovation from Physio Control.

As all electrode pads are single-use only and a key component for ensuring your AED is able to deliver a life-saving shock, it is important for you to have a spare set stored in your rescue kit to ensure your device can always be used to save a life.

LIFELINKcentral™  

The CR2 is designed to make the maintenance of your AED easier than ever before, allowing you to manage the upkeep of your device to ensure it is always ready to be used in an emergency.

Thanks to the embedded WiFi, you’ll be automatically connected to the LIFELINKcentral™  online AED management which will keep you regularly updated with the status of your AED. You will be notified 90, 60 and 30 days before your accessories are due to expire, allowing you to make new purchases in time.

Once you’ve replaced your electrode pads, a new expiry date and status will automatically update on your online AED Management page, allowing you to monitor its status both remotely and on the device itself.

More information

Want to find out more about the Physio Control LIFEPAK CR2 Replacement Electrode Kit? Simply call the defibshop team on 800 989 7768 to get the answers to your questions. 

 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.