Schiller Fred Easyport Child Pads
Schiller Fred Easyport Child Pads
Product Code 2.155062ie
- 1 pair Schiller Child Pads for use with Fred Easyport
By connecting these Fred Easyport Child Pads into your device, you transform your AED into a unit suitable to deliver a shock to a child ages 1-8.
If your AED is kept in a location which is often populated with children, we advise you keep a spare set of paediatric pads with your defibrillator to ensure you can deliver the definitive treatment against cardiac arrest to a child if needed.
- Smaller surface area suitable for the size of a child
- Up to a 2 year shelf life
- Helpful visual instructions to assist with pads placement
Sadly 12 young people die each week due to sudden cardiac arrest; this is a number which can be reduced if the correct treatment is provided. This is why having AEDs readily available along with the correct equipment to complete a rescue is so important for workplaces, schools and communal areas.
Electrode pads are essential for your defibrillator to deliver a shock to a patient, as all pads are single use only we do advise that you keep a spare set with your defibrillator so that you’re never left without in an emergency situation.
If unused your electrodes will expire in 2 years, by signing up to our free reminder service you’ll be contacted by a member of our team when you’re due to replace your pads so that you can always have confidence that your AED is rescue ready at all times.
Get in touch
If there’s anything you would like to learn more on, whether it’s our electrodes or another product from our range; get in touch with our defibshop team who are always on hand to assist with any questions you may have.
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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.