FR3 Philips Rigid System Case
FR3 Philips Rigid System Case
Product Code 989803149971
- FR3 Philips Rigid System Case
To protect your Philips Heartstart FR3 AED, this Rigid System Case has been designed specially to protect your unit in extreme environments such as the Fire Service, EMS, the military or heavy industries.
Created using the most durable plastic, this case will protect your FR3 AED and its contents against harsh elements. A Pads Sentry is included in the case so the AED’s electrodes can be tested and stored safely for quick retrieval; the case is also designed with room for the FR3 Fast Response Kit, along with a spare set of electrode pads, a spare battery pack, and even an Infant / Child key.
Dimensions: 13.2” x 10.3” x 5.2“
How to Use
If you work in an environment that can often be exposed to harsh environmental factors, keeping your portable AED safe is vital to ensure its sufficiently protected against drops, water and dust so it can provide an effective rescue in the event of a cardiac arrest.
With enough room for your accessories and additional equipment alongside your AED, you can help to save time when prepping for a rescue by having all of your essential materials in one place, ready to go.
Interested in the FR3 Philips Rigid System Case? You can call the defibshop team on 800 989 7768 with any questions you might have prior to purchase.
As an independent supplier of AEDs and accessories, you can have confidence that the advice we provide is honest and impartial, helping you to make a decision that will suit both your needs and budget.
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.