Fred Easyport Child Pads
Fred Easyport Child Pads
Product Code 2.155062
- 1 pair Schiller Child Pads for use with Fred Easyport
These paediatric pads are designed to work alongside the Fred Easyport Defibrillator. It is useful to have paediatric pads as well as adult pads stored with your defibrillator, because children aged 1 to 8 years old require a shock with lower levels of energy.
- Smaller surface area suitable for children
- Electrode pad life of 2 years
How to Use
Once you have taken the child’s pads out of the sealed wrapping, follow the instructions provided to position the pads correctly. The defibrillator will detect when the pads are in place and then administer the life-saving shock.
We aim to provide the best service available; therefore we will send you a reminder directly to your email address when the pads are due to expire. Giving you time to restock your accessories, so that your defibrillator is ready to go.
Once you use your pads, they must be replaced to ensure that they are as effective as possible. If you happen to use them within the first two years after purchase, we will send you a replacement free of charge.
About the Manufacturer
Schiller is a global supplier of electrocardiographs, patient monitors, blood pressure and ECG recorders, medical IT solutions, spirometers, and external defibrillators. They are renowned for their compact defibrillators that are considered pocket sized.
Do you need any further information about the Fred Easyport Child Pads? We are more than happy to deal with any enquiries you may have. Contact our defibshop team on 0845 071 0830.
Want to know why you should choose us? Press play and find out more...
And if it couldn't get any better..
- We have over 50 different defibrillators available and we can help you decide the best one for you
- We have over 200 trainers nationwide to deliver nationally accredited training in the use of a defib and CPR
- Over 20 staff on hand to offer impartial advice on all things defibrillators
- 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
Did we also mention we are an Award Winning company?
We’re sure that you have been past our Home Page, but in case you haven’t, skipping the intro and getting stuck into the world of defibrillators, we are an award winning company.
This year we added an impressive trophy to the cabinet by being listed 22nd in the ‘Great Place to Work: Best Workplaces 2014’ Small Business Category.
We also have to our name Salford Business Excellence Award Runner Up 2014 & 2012, Investors in People – Bronze Award and an Insight 100 Customer Service Award in Training Services 2013 award.
We also have a number of accreditations under our belt, including being a TQUK Diamond Approved Centre, ISO 9001 and 14001 and CIEH.
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.