AED Pro 2010 Guidelines Upgrade Kit


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AED Pro 2010 Guidelines Upgrade Kit

Product Code 7771-000012-01

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What's Included?

  • ZOLL Administrative Software (ZAS)
  • AED Pro upgrade instructions
  • Software update acknowledgement card

Ensuring your life-saving AED has the most up-to-date treatment guidelines will ensure you’re delivering the most recently, recommended treatment for the victim of sudden cardiac arrest. 

This upgrade kit will help you upgrade your ZOLL AED Pro to be fully compliant with the American Heart Association’s most recently released guidelines.

This kit requires the use of an infrared port (IrDA) as this will enable communication between your AED and the computer, enabling the upgrade.

About the Manufacturer

ZOLL’s story starts in 1952 at Beth Israel Hospital with the Chief of the Cardiac Clinic, Paul M. Zoll, M.D.

During this time, he demonstrated the positive effects of external defibrillation on a heart that had entered into a dangerous arrhythmia, causing the cardiac arrest.

Since then, thanks to their bright and bold green designed AEDs, ZOLL has gone on to become one of the world’s most recognized AED manufacturers.

Each and every device designed by ZOLL has ease of use at the center of the design, so no matter what level of training you’ve had with AEDs, you can confidently deliver the life-saving treatment required by a cardiac arrest victim.

More Information

If you require further information about the AED Pro 2010 Guidelines Upgrade Kit, get in touch with one of our friendly advisors in the defibshop team.

Simply call 888 820 0760 and one of our team members will be happy to assist you with any questions you may have. 

 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.