Physio Control LIFEPAK 20e Defibrillator/Monitor with Pacing Package


Additional Images

  • LIFEPAK-20e-Defibrillator-Monitor-Pacing-SpO2-Package
  • LIFEPAK-20e-Defibrillator-Monitor-Pacing-SpO2-Package

Physio Control LIFEPAK 20e Defibrillator/Monitor with Pacing Package

Product Code 70507-000080

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In Stock

What's Included?

  • Physio-Control LIFEPAK 20e Defibrillator/Monitor with Pacing Package
  • LIFEPAK 20e QUICK-COMBO electrodes with REDI-PAK pre-connect system
  • LIFE-PATCH ECG adult electrodes pack (3 electrodes per pack)
  • Rescue Kit
  • 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 enable ACLS-trained Clinicians to administer cardiac care. This unit has additional features to enhance your hospital’s ability to effectively manage resuscitations from preparedness through review.

The LIFEPAK 20e defibrillator/monitor is extremely intuitive for the first responder, and also skilfully combines AED function with manual capacity so that ACLS-trained clinicians can quickly and easily deliver advanced therapeutic care. The CodeManagement Module adds waveform capnography and wireless connectivity to enhance your hospital’s ability to effectively manage resuscitations from preparedness review. 

Unique Features

Dual-mode design

The 20e unit features a dual-mode design that allows for both manual and AED use. This allows the unit 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.

About The Manufacturer 

Physio-Control work to save lives and their AEDs have set the standard for six decades, saving tens of thousands of lives. Priding themselves as the pioneers of research and innovation in the defibrillator industry, they are a world leader in the development, manufacture, sale and service of AEDs and are widely trusted by healthcare professionals and first responders.

More Information

If you would like to know more about The LIFEPAK 20e defibrillator/monitor with pacing package just get in touch and a member of the team will assist you with any questions or queries you may have. Just call 800 989 7768.

 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.