AED Plus 2010 Guidelines Upgrade, Single Kit (CD and One Overlay Label Set)

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AED Plus 2010 Guidelines Upgrade, Single Kit (CD and One Overlay Label Set)

Product Code 7771-000011-01

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What's Included?

  • ZOLL Administrative software
  • One overlay label set
  • Overlay label placement instructions
  • AED Plus upgrade instructions
  • Software update acknowledgement card

ZOLL’s AED Plus 2010 Guidelines Upgrade, Single Kit will enable ZOLL AED Plus owners to upgrade their devices to the 2010 American Heart Association’s treatment guidelines, meaning if the device is to be used in a rescue, the rescuer will be providing treatment inline with the 2010 guidelines.

Updating your ZOLL AED Plus to the 2010 treatment guidelines will ensure that responders are delivering treatment inline with these guidelines, providing the most effective care for the patient and the highest chance of survival.

The overlay labels are to be used to modify the icons on the face of the ZOLL AED Plus to be in line with the 2010 treatment 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

Dating back to 1952, ZOLL Medical has dedicated their time to developing and manufacturing AED Technologies for over 60 years. This all started with the Chief of the Cardiac Clinic at Beth Israel Hospital, Paul M. Zoll, M.D.

Over time, they have become famous for their bright green devices that stand out in almost any environment and allow almost anyone to use the devices in a time of need, with confidence.

More Information

If you would like to learn more about the AED Plus 2010 Guidelines Upgrade, Single Kit (CD and One Overlay Label Set), speak to the team here at defibshop.

Simply call 888 820 0760 to speak to one of our friendly experts and they’ll be happy to assist 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.