ZOLL AED Pro Non-Rechargeable Lithium Battery
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ZOLL AED Pro Non-Rechargeable Lithium Battery
Product Code 8000-0860-01ie
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What's Included?
- Non-rechargeable Lithium Battery
This replacement battery pack will help to ensure your ZOLL AED Pro AED is rescue ready at all times in the event of a cardiac arrest.
In addition to giving your defibrillator the power to provide a defibrillation shock to a casualty, a working battery will allow your device to carry out important routine self-checks to ensure all elements in the device are in optimum working condition and ready for use.
Additional Features
- Battery is disposable after use
- Maximum 5 year battery life
- Automated self checks
Helpful Tips
You will be alerted to low battery power by your AED thanks to its automated checks; a battery is a core accessory for a working defibrillator which is why we always recommend you keep a spare with your device to ensure it’s always rescue ready.
As most battery’s have an expiry date, we find registering with our free reminder service is a stress-free way of ensuring your AED is always equipped with the vital equipment required. Simply register the details of your battery with us and as your expiration date approaches, we’ll send you a reminder email and how to repurchase to ensure your device is never without a working battery.
About the Manufacturer
ZOLL develops and markets medical devices to help with emergency care and to save lives. They produce equipment for defibrillation, therapeutic temperature management, fluid resuscitation, data management and for monitoring circulation and CPR feedback.
More Information
Do you require any further assistance? No problem. Contact ourdefibshop team today and they will provide you with honest and expert advice.
Want to know why you should choose us? Press play and find out more...
Buying a defibrillator? You’ve come to the right place...
- With nearly 20 different defibrillator models available, our defibshop team knows them all and can help you decide which device suits your budget, environment and business
- We have over 20 staff on hand who can offer friendly and impartial advice on all things defibrillators
- Not only do we provide a free battery and electrode pad reminder service, but we will replace your electrode pads for free if they are used within two years of purchase
Did you know that we're an Award Winning company?
We’re not a company for bragging but we like to think that our trophy cabinet indicates that you have come to a trustworthy and dependable company who recognises you are making a significant and fantastic step when buying a defibrillator.
We were recently listed in the Small Business category of the 'Great Place to Work: Best Workplaces 2014’ whilst we have also won accolades in the Salford Business Awards 2014 & 2012, Investors in People Bronze award and an Insight 100 Customer Service Award in Training Services 2013.
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.
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