ZOLL AED Pro Non-Rechargeable Lithium Battery

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ZOLL AED Pro Non-Rechargeable Lithium Battery

Product Code 8000-0860-01USA

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What's Included?

  • AED Pro Non-rechargeable Lithium Battery

For use with the Zoll AED Pro, this non-rechargeable Lithium Battery is a vital part of your AED kit. Without a charged battery, your AED cannot power the defibrillation shocks to help rescue a victim of cardiac arrest.

Features

  • Disposable
  • Lasts 5 years
  • Automated self-checks

How to Use

Install the battery following the instructions provided by the product manual. Once the battery has been inserted, your device will automatically begin to perform its automated checks to ensure the defibrillator is working exactly as it should.

These tests will take place on a daily, weekly and monthly basis, alerting you if anything requires your assistance.

In order to activate the kit for a rescue, simply attach the pads and turn on the AED. The unit will use voice prompts to direct you through the process.

Once the battery loses power, the defibrillator should detect this during one of the automated checks. It will alert you with the audio message ‘change battery’. This is why we advise for you to keep a spare battery with your AED at all times.

More Information

Got a question to ask before you purchase? Or maybe you need help finding the right product for you, no matter what your concern; the defibshop team are here to help. Simply call 800 989 7768 to speak directly with one of our advisors.

 

 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.