USB Clinical Event Download Cable

USB Clinical Event Download Cable

Product Code 8000-000865

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What's Included?

  • USB Clinical Event Download Cable

Designed for use with ZOLL AED Pro or X Series AED’s, this cable will allow you to download important cardiac arrest event data from your life-saving AED to recall specific events from the rescue. 

By using a data cable, important rescue information can be retrieved and studied by the emergency services who can then go on to determine the underlying cause for the cardiac arrest.

About the Manufacturer

ZOLL’s history dates back to the 1950’s when founder, Dr. Paul Zoll discovered the positive effects external defibrillation could have on a heart that has entered into cardiac arrest.

Thanks to their bold and bright green designs, ZOLL AEDs are sure to stand out in almost any public environment, thus eliminating any delays that may hinder treatment being delivered to the victim of cardiac arrest.

All of ZOLL’s devices have been designed with ease of use and professionalism in mind. So, regardless of whether you’re a first-time responder or a medical professional, you can have confidence in the treatment you’re delivering to the casualty whilst using a ZOLL AED.

Get in touch

If you require more information about the USB Clinical Event Download Cable, the defibshop team are here to answer any questions you may have.

To get in touch with one of our advisors, simply call 800 989 7768 and one of our team members will assist you in any way they can. 

 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.