Ready Kit

Cardiac-Science-Ready-Kit

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  • Cardiac-Science-Ready-Kit

Ready Kit

Product Code 5550-004USA

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In Stock

What's Included?

  • Ready Kit

This Ready Kit has been designed to assist both trained and untrained rescuers to help them prepare the patient for defibrillation.

The kit includes a pair of scissors which can be used to remove any clothing, as well as a razor to remove any excess hair which may impede the effectiveness of the electrode pads stickiness when being placed on the patient.

You’ll also find equipment such as a CPR mask and facial wipes which are included to help protect the rescuer and victim from infection.

The contents of this kit will help improve the efficiency of your rescue, ensuring that the treatment delivered is both safe and effective for the patient.

About the Manufacturer

Cardiac Science’s AED ranges are designed to assist both medical professionals and untrained users alike with the life-saving treatment delivery, by making the process as easy and as simple as possible.

As a brand, they are committed to raising awareness about the positive effects of these devices by public access defibrillator programs which have been run through various communities in the USA. This is just a small indication of their commitment to saving lives. 

More Information

Want to learn more? Get in touch with the friendly defibshop team on 888 820 0760 and one of our friendly customer service advisors will be happy to answer any questions you may have.

 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.