Physio Control Lucas 3.1 Training Unit


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Physio Control Lucas 3.1 Training Unit

Product Code 99576-000083

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What's Included?

  • LUCAS 3, v.3.1 Training Unit

The latest in training units, the LUCAS 3.1 Training Unit allows users to practice chest compressions on a manikin.

Performing CPR within the first 3-5 minutes can increase a victim’s chance of survival from 6% to 74%. Immediate CPR is made even more effective when delivering high-quality chest compressions with a depth of 2 inches and a rate of at least 100 compressions per minute.

The latest version of the LUCAS Training Unit provides trainees with all the knowledge they’ll need to use the clinical version of the device during a real cardiac emergency by allowing them to experience the unit in action on a manikin.

Key Features

  • Default Settings: 102+/- 2 compressions per minute
  • Suction cup for assistance in recoil to start position
  • Piston to stabilize compression points
  • Wireless Connectivity (to the LIFENET System)

How to Use

This training unit, provides users with first-hand experience of how the clinical counterpart to the LUCAS 3.1 Training Unit would react during an emergency.  

The user simply needs to place the manikin in place of where the patient would be and lower the compression device until it is resting in the center of the patient’s chest. It will then begin continuous effective CPR.

By the compression system delivering CPR, it frees up the responder to effectively complete other essential tasks, such as preparing the AED to deliver a potentially life-saving shock or calling the EMS whilst the system continually performs CPR.

About the Manufacturer

Physio-Control has worked to save lives for six decades, saving tens of thousands of lives with their innovative AEDs.

Famous for their Lifepak AED range, devices from Physio Control are developed and manufactured to a high standard and boast simplistic user-interfaces, allowing both trained and un-trained responders to act with confidence in the event of an emergency.

For More Information

Do you have questions about the LUCAS® 3 Training Unit or would like to learn more about how high-quality CPR can save a life? Our team is here to help. Give us a call at (888) 820-0760 and speak with a team member today.

 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.