Physio Control LIFEPAK 15 Trending, Masimo SpO2, NIBP, EtCO2, 2 Invasive Pressure Channels, Bluetooth


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Physio Control LIFEPAK 15 Trending, Masimo SpO2, NIBP, EtCO2, 2 Invasive Pressure Channels, Bluetooth

Product Code 99577-001959

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In Stock

What's Included?

  • LIFEPAK 15 monitor/defibrillator
  • AED/ manual defibrillation
  • 12 Lead ECG monitoring capability and cable
  • 8.4" Colour LCD Display
  • SPO2 (measuring oxygen saturation levels)
  • NIBP (non-invasive blood pressure monitoring)
  • Bluetooth

The LIFEPAK 15 monitor/defibrillator is for clinical use, offering the most clinically innovative and operationally effective device available. The LIFEPAK 15 offers sophisticated clinical technologies with advanced features.

The most advanced unit is needed for responding to emergencies. An AED that sets the standard in toughness, operations and innovation. The LIFEPAK 15 offers exactly that; with an impressive IP rating, this durable device will still work no matter how harsh the environment is, whether it is dropped, wet or dirty.

Key Features

  • Advanced monitoring parameters
  • Advanced support for treating cardiac patients
  • Full energy, up to 360 joules for patients that need it
  • CPR guidance and post-event review
  • Dual-mode LCD screen with SunVue™ display     
  • Flexible power options
  • Data connectivity
  • Upgradable platform
  • IP rating of 44 meaning high protection against dust and water

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

Would you like to know more about the LIFEPAK 15 or any of our other products? Our helpful defibshop team are on hand to answer any questions you may have before you make your life-saving investment. You can call 800 989 7768 and a member of the team will happily answer any 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.