AED Plus 2010 Guidelines Upgrade, CD ONLY.


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AED Plus 2010 Guidelines Upgrade, CD ONLY.

Product Code 7771-000013-01

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What's Included?

  • ZOLL Administrative software
  • AED Plus upgrade instructions
  • Software update acknowledgement card

The AED Plus 2010 Guidelines upgrade from ZOLL provides you with the CD required to update your ZOLL AED Plus to the 2010 guidelines from the American Heart Association.

Ensuring your ZOLL AED Plus has the latest software installed will help ensure that when the device is used in a rescue, the responder will be providing the latest and most up-to-date treatment for the patient, in line with the AHA’s 2010 guidelines.

ZOLL’s administration software (ZAS), is compatible with the following systems:

  • Windows XP
  • Windows 2000
  • Windows Vista
  • Windows 7

Please note: this software is not compatible with Mac OS.

About the Manufacturer

Born in 1952, ZOLL Medical has been designing and manufacturing AED technologies for over 60 years and it all started with the Chief of the Cardiac Clinic at Beth Israel Hospital – Paul M. Zoll, M.D.

Since then, their devices have become some of the world’s most recognized AED devices, thanks to the bright green design which will ensure the AED can stand out in almost any environment.

More Information

If you require more information about the AED Plus 2010 Guidelines Upgrade, CD Only, the defibshop team are here to help.

To get in touch with one of our advisors, call 888 820 0760 and they’ll be happy to help.

 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.