Philips FR2 Replacement Long-Life Battery

FR2-Replacement-Long-Life-Battery

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Philips FR2 Replacement Long-Life Battery

Product Code m3863ausa

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In Stock

What's Included?

  • Long-Life Battery for use with the FR2

For use with your Philips FR2 AED, this long-life lithium manganese dioxide battery will ensure your unit has sufficient power to provide effective defibrillation to a victim of cardiac arrest.

Being the sole power force for your AED, a battery is one of the core components of your unit, ensuring it works exactly as it should in the event of an emergency. 

Core Accessories

As well as providing the power to defibrillate a victim of cardiac arrest; a fully-charged battery will allow your device to carry out its daily, weekly and monthly self-checks. These checks are important to help you keep on top of the maintenance of your device, which will alert you to any issues which require your attention via flashing indicator and/or audible alarm.

These issues can be anything from low battery levels to disconnected electrode pads; the self-checks ensure you know as soon as any issues arise, allowing you to rectify them, prior to AED use. This ensures your unit is always is a state of readiness and can deliver a rescue, should an SCA occur.

This FR2-series battery has a shelf life of 5 years, plus a typical standby life of 5 years (4 years minimum).

More Information

Got a question about the FR2 Long Life Battery? Whether you’re looking for more advice on this product or any other item on our website, please contact our helpful Product Specialist team by calling 800 989 7768. 

 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.