Cardiac Science Powerheart G5 Reusable Training Pads with CPR Device (Adult)

Powerheart-G5-Reusable-Training-Pads-with-CPR-Device-Adult

Additional Images

  • Powerheart-G5-Reusable-Training-Pads-with-CPR-Device-Adult

Cardiac Science Powerheart G5 Reusable Training Pads with CPR Device (Adult)

Product Code XTRPAD002AUSA

0 reviews

In Stock

What's Included?

  • 1 set of G5 reusable training pads with ICPR 

Compatible with the Powerheart G5 Training Unit AEDs, these electrode pads are identical to their clinical counterparts and can be reused multiple times on any CPR manikin. 

The G5 Reusable Training Pads with CPR Device can be used on any Powerheart G5 Training unit and will help you provide your learners with the most realistic training scenarios as they replicate the same features as their medical counterparts.

Providing a real-life scenario for your learners will enhance their learning experience and boost their knowledge of AEDs and what steps to take should someone fall victim to sudden cardiac arrest.

Key Features

  • Can be used on any training manikin
  • Reusable
  • Added CPR Device provides learners with feedback on their CPR compressions
  • Similar design to clinical pads to enhance the learners training and understanding
  • Clear, easy to understand images help the learner to place the pads correctly on the manikin
  • Designed specifically for use with the Powerheart G5 AED Training units

How to use

Designed to be used in the exact same way as their clinical pad counterparts, simply apply the electrode pads to the manakins chest, as per the diagrams and follow the audio steps provided by the AED. These pads come pre-packaged, similarly to the clinical electrodes and can also be pre-connected to enhance the learner’s training experience.

The additional CPR device provides chest compression feedback to the learner. This helps to highlight the importance of effective CPR in a real life cardiac emergency.

More Information

Want more information about the Powerheart G5 Reusable Training Pads? The defibshop team are always on hand to help you.

Our advisors are experts in their field and are happy to share their knowledge with you. Call them on 800 989 7768 and they’ll be sure to find you the right product to suit your needs.

 

 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.