LUCAS 3.1 Chest Compression System

In a cardiac arrest, every second without high-quality chest compressions reduces the chance of survival. Manual CPR, however well-trained the responder, deteriorates in quality within minutes, due to physical fatigue, patient transport movement, or the sheer demands of a multi-casualty or prolonged resuscitation scenario. For the teams that cannot afford that deterioration, the Stryker LUCAS 3.1 Chest Compression System is the established clinical standard.

The LUCAS 3.1 is the world's most used automatic CPR machine, an automated chest compression device that delivers consistent, guideline-compliant compressions without the limitations of manual CPR.

Having a device that automatically delivers chest compressions means a more efficient use of rescue staff time, as usually teams of two must cycle between rounds of CPR if done over longer periods.

The LUCAS 3.1 even allows for adjustable compression rates at the touch of a button, in compliance with the Resuscitation Council UK's guidelines of over 100 compressions per minute. Plus, a post-event report records all compression rates, depth, and duration for complete transparency.

Included with the LUCAS 3.1 device is the carry case, enabling rescue staff to transport the machine over rugged terrain easily.

Please note: the LUCAS 3.1 is dispatched to order with a lead time of several weeks and orders are non-cancellable. The auxiliary power supply is sold separately. 

For all enquiries about the Stryker Lucas 3.1 Chest Compression System, please contact us on 01298 872 186 or use the web chat to speak with one of our specialists.

Necessary Accessories for the LUCAS 3.1

LUCAS 3.1 Chest Compression System Auxiliary Power Supply

Recommended LUCAS 3.1 Products

LUCAS 3.1 Chest Compression System Battery

LUCAS 3.1 Chest Compression System Carry Case

Helpful Stats: CE marked as a Class IIb medical device, Stryker has deployed over 50,000 units globally, with a patient treated by a LUCAS device approximately every minute worldwide. More than 200 peer-reviewed publications underpin its safety and efficacy. The LINC randomised controlled trial, published in the Journal of the American Medical Association, demonstrated the device's ability to deliver consistent compressions across 2,589 pre-hospital cardiac arrest patients. In real-world clinical use, the LUCAS 3.1 transitions from manual to mechanical CPR in a median of 7 seconds, with greater than 99% documented operational reliability. More than 99% of survivors treated with the LUCAS device had good neurological outcomes at six months follow-up.