Physio Control Lifepak 15 Defibrillator with 12-Lead ECG – Recertified


Additional Images

  • Lifepak-15-recertified-12-lead-ECG

Physio Control Lifepak 15 Defibrillator with 12-Lead ECG – Recertified

Product Code PHYLP1512BIPSBCA-V2-R

0 reviews

In Stock

What's Included?

  • LIFEPAK 15 monitor/defibrillator
  • Lifepak 15 AC Power adapter- recertified
  • AED/ manual defibrillation
  • 12-Lead ECG monitoring capability and cable
  • 8.4" Colour LCD Display
  • Bluetooth

This is a fully-loaded unit from Physio-Control. The Lifepak 15 boasts an impressive array of parameters, including 3-Lead ECG, Rainbow SpO2, NiBP, EtCO2, and Bluetooth. 

The unit also comes with a Lifepak 15 AC power adapter that is also recertified. The latest version of the Lifepak 15 includes new features that complement the existing features of the defibrillator.

Unique Features

The Lifepak 15 sets the new standard in clinical innovation:

  • New monitoring parameters
  • Advanced support for treating STEMI patients 
  • Most potent escalating energy available
  • Proven CPR guidance

The Lifepak 15 sets a new standard in operation innovation:

  • Dual-mode LCD screen with SunVue
  • Upgradable platform
  • Data Connectivity
  • Latest Lithium-ion battery technology
  • Attention to detail

The Lifepak 15 is also the new standard in Lifepak Tough:

  • IP44 rating
  • Toughened inside and out

More Information

If you have any questions regarding the Physio-Control Lifepak 15 defibrillator with 3-lead ECG-Recertified do not hesitate to contact a member of the team for more information. Get in touch by calling 800 989 7768.

  • Dimensions
    18 × 18 × 18 in
  • Weight

 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.