FR3 Small Soft Case


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  • FR3-Small-Soft-Case

FR3 Small Soft Case

Product Code 989803179191ie

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In Stock

What's Included?

  • Small Soft Case
For use with Philips HeartStart FR3 AED, the Small Soft Case has been designed with ultimate portability in mind.

This case is for use with the Philips Heartstart FR3 AED. The case has been produced with portability in mind- its compact design is light and made of a soft material, enabling you to carry it quickly and easily to the patient. A Pads Sentry is incorporated so that the electrode pads can be stored safely and tested for fast deployment.
The great thing about this case is that it has an Auto-On function. When you open the case the defibrillator automatically switches on, enabling swift treatment.

How to Use

This case is similar to the rigid version because it also has specific storage for other accessories such as spare pads and batteries, as well as potential space for the Infant/ Child key to quickly switch the AED to the paediatric function.

Use the case to store the defibrillator and accessories in one place, and you will minimise the time wasted in a situation where every second counts towards saving a person’s life.

About the Manufacturer

Philips have been developing innovative technologies for over 120 years. They provide technology for a number of sectors including healthcare, and have become a very popular brand in the defibrillator industry.

More Information

Want to know more about the FR3 Small Soft Case? No problem. You can contact our defibshop team for more details about this product and any others featured on our website.


 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.