ZOLL SeeThru CPR Simulator for E Series, R Series, and AED Pro

ZOLL SeeThru CPR Simulator for E Series, R Series, and AED Pro

Product Code 8009-0751-01

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What's Included?

  • SeeThru CPR Simulator for E,R Series and AED Pro

Designed for use with the ZOLL E Series, R Series and AED Pro, the SeeThru CPR Simulator enables you to simulate various cardiac emergencies to display how the AED would react in a real-life situation. 

The SeeThru CPR Simulator allows you to provide the most realistic training experience for your first aid students by displaying to them how the AED would react at each stage of a real-life rescue process.

Simulating various emergencies will provide a further insight into what would be required in a real-life scenario, boosting their confidence in their actions if treatment was required by a casualty.

About the Manufacturer

Since Dr. Paul Zoll demonstrated the effects external defibrillation could have on a victim of cardiac arrest, ZOLL has gone from strength to strength.

Their easily recognizable, green AEDs have helped them become one of the world’s most well-renowned manufacturers in the world.

Every AED designed and manufactured by ZOLL has been created with ease of use in mind, so regardless of your training level, you can feel confident whilst delivering treatment to the patient when using a ZOLL AED.

More Information

If you would like more information on this product or any other product listed on our website, please don’t hesitate to get in contact with the defibshop team.

Simply call 888 820 0760 and one of our knowledgeable 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.