ZOLL Replacement Gel Pads for Training CPRD-Pad - Set of 5

Replacement-Gel-Pads-for-Training-CPRD-Pad-Set-of-5

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ZOLL Replacement Gel Pads for Training CPRD-Pad - Set of 5

Product Code 8900-0803-01USA

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What's Included?

  • 5 sets of replacement gel pads for Training CPRD-Pad 

For use with Zoll AED Training Units, these replacement training electrode pads can be applied to first aid manikins to help provide the most realistic training experience possible.

The unique shape of the Zoll Electrode Pads helps users to provide the most effective chest compressions possible. Not only do the pads have clear diagrams for pad placement, but the CPR aid measures the rate and depth of compressions and will prompt the responder to push harder or faster if required.

Pad Features:

  • Pre-connected to save time
  • Visual aids to help with pad placement
  • Disposable packaging
  • Extra sticky adhesive
  • The Z shaped pattern of the pad- a one piece electrode- saves valuable time when applying to the patient’s chest

How to Use

These pads are designed to be used specifically with training units and cannot be used on a functioning AED. Potential users can use this training accessory to practice where to place the pads on resuscitation dolls in a rescue scenario.

Follow the diagram provided on the pads to place the electrodes exactly where they should be on a victim. Once positioned correctly, the training AED will then be able to analyze the “patient’s” heart rhythm just as a clinical unit would and will provide a shock if required.

Its improved polymer gel adhesive provides this accessory with a 5 year shelf life – currently the longest on the market!

More Information

Thinking of purchasing this product? Feel to contact our helpful team of AED experts if there are any questions you’d like to ask first.

Call 888 820 0760 to get in touch with a defibshop advisor direct.

 

 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.