Physio Control LIFEPAK 20e Defibrillator/Monitor


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Physio Control LIFEPAK 20e Defibrillator/Monitor

Product Code 70507-000061

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In Stock

What's Included?

  • Physio-Control LIFEPAK 20e Defibrillator/Monitor
  • LIFEPAK 20e QUICK-COMBO electrodes with REDI-PAK pre-connect system
  • Rescue Kit
  • LIFE-PATCH ECG adult electrodes pack (3 electrodes per pack)
  • LIFEPAK 20e 3-Lead ECG cable
  • QUICK-COMBO therapy cable
  • QUICK-COMBO test plug
  • LIFEPAK 20e A/C power cord
  • Box of ECG printer paper (includes 3 rolls of 50 mm x 30 m)
  • LIFEPAK 20e Defibrillator/Monitor Owner's Manual
  • LIFEPAK 20e Defibrillator/Monitor CD-ROM service manual
  • 5 Year Warranty

The LIFEPAK 20e AED is a clinically advanced unit that will allow ACLS-trained Clinicians to administer cardiac care.

Time is precious when it comes to responding to a sudden cardiac arrest. In-hospital first responders that are equipped with a LIFEPAK 20e AED will be able to make the life-saving difference for patients that have suffered a cardiac arrest. 

The LIFEPAK 20e Defibrillator/Monitor is a highly intuitive unit to use, it combines an AED function for the BLS-trained responder, with manual capability so that ALS-trained clinicians can quickly and easily deliver advanced diagnostic and therapeutic care; two AEDs in one if you like.

Unique Features

Dual-mode design

The 20e unit features a dual mode design for both AED and manual use. Allowing it to be used as a simple yet effective AED for first responders, but can easily transform into a manual AED for advanced care professionals to deliver treatment based on their medical knowledge.

More Information

If you would like to know more about the LIFEPAK 20e Defibrillator/Monitor, our team would love to help. Get in touch by calling 800 989 7768 with any questions or queries 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.