CU Medical iPAD Li-ion Disposable Battery Pack


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  • iPAD-Li-ion-Disposable-Battery-Pack

CU Medical iPAD Li-ion Disposable Battery Pack

Product Code 63010ie

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What's Included?

  • iPAD Li-ion Disposable Battery Pack

Designed for use with the iPAD NF1200 defibrillator, this disposable Li-ion battery pack will ensure that your AED is always ready for use.

To ensure your life-saving device is in optimum working condition, it is essential that the device is equipped with a full battery pack as this will ensure it can be used to provide treatment to a victim of Sudden Cardiac Arrest as well as perform the vital maintenance checks on a daily, weekly and monthly basis.

The battery will power the defibrillator and even if you haven't touched the device for more than a day, the device will still perform the important daily, weekly and monthly self-checks to ensure it can be used in a cardiac emergency.

Key Features

  • Designed for exclusive use with the NF1200 defibrillator range
  • Shelf life of up to 5 years
  • Ensures the device can perform the required self-tests
  • Provides a minimum of 120 shocks or 4 hours of operating time
  • Disposable

How to Use

Once you have clicked the battery, you're all set and ready to go. The unit will now be able to be used in a rescue as well as perform the self-checks required to ensure every part of the device is in working order.

Essential self-checks ensure that the electrodes, hardware, software and subsystems are all fully operational and ready for use at a moment's notice.

More Information

If you would like to learn more the team here at defibshop will be happy to help.

Call 015079907 and one of our friendly experts will happily share their expertise with you.

 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.