Physio Control Electrode EDGE QUIK-COMBO Adult

Physio Control Electrode EDGE QUIK-COMBO Adult

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Physio Control Electrode EDGE QUIK-COMBO Adult

Product Code 11996-000091

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What's Included?

  • Electrode EDGE QUIK-COMBO Adult

Designed for use with the Physio Control LIFEPAK 12, 15 and 20 devices, the Electrode EDGE QUIK-COMBO have been designed for a single patient application.

From Physio Control, the Electrode EDGE QUIK-COMBO Adult are designed for single patient application and are capable of performing ECG monitoring, noninvasive pacing, defibrillation, and synchronized cardioversion through one set of electrode pads.

Unique EDGE System(TM) technology results in even current distribution, helping to reduce the risk of skin burns.

Please note: these electrode pads have the lead wires inside the foil packaging and are unable to be "pre-connected" to the device.

About the Manufacturer

Physio Control's range of life-saving technologies has been designed to suit the professionals and the first time responders.

Famous for their LIFEPAK range, AEDs built by Physio Control combine medical-grade technology with a simple, user-friendly shell, allowing responders of all levels to use the devices in emergencies and feel confident while delivering the treatment.

More Information

If you would like more information about the Electrode EDGE QUIK-COMBO Adult, get in touch with the team here at defibshop.

Call 800 989 7768 and one of our experts will be happy to share their knowledge with you.

 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.