Inservice DVD Rom Assy LP20E with CMM

Inservice DVD Rom Assy LP20E with CMM

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Inservice DVD Rom Assy LP20E with CMM

Product Code 26500-003545

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What's Included?

  • Inservice DVD Rom Assy LP20E with CMM

To fully understand the features, functions and controls of Physio Control’s Lifepak 20e, the Inservice DVD ROM will provide you with all the information you require. 

Ensuring your AED is able to save a life and continually monitor the patient after the potentially life-saving shock has been delivered is essential; the Lifepak 20e’s Inservice DVD ROM will help ensure you have a thorough understanding of your device as well as how it works and assists the rescuer.

About the Lifepak 20e

Physio Control’s Lifepak 20e AED/ monitor is a cardiac emergency response system, designed for use by trained, authorized medical professionals in clinical and hospital settings.

Available with additional options, including semi-automatic configuration, noninvasive pacemaker, pulse oximeter and paddle accessories, you can have confidence in the fact that the Lifepak 20e system will provide you with everything you require as a trained professional to act in a cardiac emergency.

More Information

If you require more information about the

If you would like more information about the INSERVICE DVD ROM ASSY, LP20E WITH CMM, the defibshop team are the ones to speak to.  

To speak to one of our friendly, knowledgeable advisors, call 888 820 0760.


 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.