Cardiac Science Powerheart G5 Ready Kit

Cardiac Science Powerheart G5 Ready Kit

Product Code UKIT001A

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In Stock

What's Included?

  • Nitrile gloves (M/L)
  • Razor
  • Scissors
  • Paper towel (x 2)
  • Gauze 
  • One-way filter CPR mask

Designed to assist you with your rescue alongside the Powerheart G5 AED, you can store your G5 Ready Kit alongside your life-saving unit for quick use in a cardiac emergency.

Gloves and a CPR mask are just some of the equipment included in the Ready Kit to help you provide quick and effective treatment whilst keeping both yourself and the casualty safe.

Also, included in the kit, you will find a towel and gauze to provide care to any open wounds the victim may have suffered, along with a razor to help you prepare the patient’s chest to enable effective electrode pad placement.

About the Manufacturer

Cardiac Science is committed to saving lives and has created a functional, easy-to-use range of AEDs to assist both medical professionals and untrained users in saving a life.

Their signature orange design is a popular choice for a range of environments and its ease of use ensures just about anyone can use the unit to help save a life.

More Information

Ready to compliment your AED unit with an effective ready kit? If you have any questions prior to purchase, you can count on our helpful defibshop team to answer any queries you may have.

To get in touch, simply call 888 820 0760 where a member of our team will happily assist you.   

 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.