Physio Control LIFEPAK 15 Trending, Masimo SpO2, SpCO, NIBP, 12-Lead ECG, EtCO2, Bluetooth

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Physio Control LIFEPAK 15 Trending, Masimo SpO2, SpCO, NIBP, 12-Lead ECG, EtCO2, Bluetooth

Product Code 99577-001957

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What's Included?

  • LIFEPAK 15 monitor/defibrillator
  • 12 Lead ECG monitoring capability and cable
  • 8.4" Color LCD Display
  • Bluetooth
  • AED/manual defibrillation

The most clinically innovative model, the LIFEPAK 15 offers users 15 technologies like advanced monitoring, system upgrades, and the most powerful escalating energy to ensure effective treatment.

Designed for use by professionals, the LIFEPAK 15 provides all the technologies and components a trained responder would require during a cardiac emergency. Thanks to continual developments, the LIFEPAK 15 will ensure innovative and effective treatment. With 15 technologies and an IP rating of 44, this device is the one of the most advanced units on the market, setting the standards in durability and operation.

Dimensions:W40cm x H31cm x D23cm

Key Features

  • Advanced monitoring capabilities
  • Upgradable platforms
  • CPR guidance and post-event reviews
  • Advanced Monitoring
  • Reaches up to 360 joules for patients that may need it
  • Data Connectivity
  • Dual-mode LCD Screen with SunVue™ display
  • Chargeable Battery

About the Manufacturer

Physio-Control has saved lives and created heart safe environments with their AEDs for six decades. As pioneers of research and innovation, their AEDs have set the standard. Famous for their Lifepak AED range, all of Physio-Control’s devices are built with trained and untrained responders in mind, providing medical grade technology in simple, easy to use devices.

More Information

Looking for more information about the LIFEPAK 15 or our other products? You can always call us at 800 989 7768 and a team member will help answer any questions 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.