Electrode Cable : reverse adapter for Medtronic defibrillators

Electrode Cable : reverse adapter for Medtronic defibrillators

Product Code 9055-001USA

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What's Included?

  • Reverse adapter electrode cable

Designed for use with Medtronic AEDs (Physio Control models) this cable enables you to connect between AEDs, allowing you to use various electrode pads with your life-saving Physio Control device. 

Using a QUIK-COMBO ® system, this accessory will allow you to use other electrode pads to deliver life-saving care in the event of a cardiac emergency.

About the Manufacturer

Physio Control’s Lifepak 1000 was selected to be the first AED to travel all the way into Space and be placed on the International Space Station. If their AEDs are good enough to be selected as the life-saving device for the ISS, they’re certainly easy enough for a first-time responder here down on Earth. 

Physio Control places ‘ease of use’ at the heart of all their technologies as this ensures both trained and untrained responders will be able to use the device in the event of an emergency. Since 1955, this has helped Physio Control to strive towards their goal of everyone living in a world where all SCA victims are successfully treated and revived.

More Information

Looking for more information on the Cable Reverse Adapter from Physio Control? The friendly, expert defibshop team are here to help.

Call us on 0000 000000 where one of our advisors will happily answer any questions you may have to help you find the right product to suit your needs.

 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.