If you are a paramedic service dealing with the fact that CPR only provides 35% of necessary blood flow — this project developed a portable, sensor-embedded catheter that extends the resuscitation window from 20 to 60 minutes.
Intelligent Aortic Balloon Catheter to Increase Cardiac Arrest Survival Rates
Imagine a smart balloon that can be placed in a major artery during a heart attack to act like a traffic controller for blood. It stops blood from going to non-essential areas and pushes it toward the brain and heart instead. This gives doctors three times as much time to save the patient compared to standard CPR.
What needed solving
Standard CPR only provides 35% of necessary blood flow, leaving survival rates stagnant at 10% and as low as 3.3% for non-shockable rhythms.
What was built
An automated Aortic Balloon Occlusion system featuring a patented sensor-embedded catheter for fluoroscopy-free positioning.
Who needs this
Who can put this to work
If you are a device maker dealing with the need for fluoroscopy-free positioning — this project developed a patented sensor system that allows safe catheter placement without X-ray machines.
If you are a hospital dealing with the 3.3% survival rate for non-shockable cardiac arrests — this project developed an automated occlusion system that could increase survival rates by up to 40%.
Quick answers
What is the projected revenue and market potential?
The device is projected to reach €931.37M in revenues by 2033. It targets a global crisis where cardiac arrest incidence is expected to rise to 11 million cases by 2030.
What is the status of the intellectual property and licensing?
The project utilizes a patented sensor system for fluoroscopy-free positioning. Based on available project data, the company is pursuing FDA De Novo authorization and global distribution partnerships.
How is the product scaling toward industrial use?
The project has transitioned from porcine models to multi-center human clinical enrollment via the ARISE trial. It has already reached TRL 7 and is moving toward commercial roll-out by 2027.
What regulatory milestones have been achieved?
The project secured a Class III CE mark from TÜV SÜD in Q3 2025 and previously leveraged a 2021 FDA 510(k) clearance.
What is the timeline for full market availability?
The commercial roll-out is projected for 2027, following the completion of the ARISE trial and regulatory authorizations.
Who built it
The project is led by a single SME, NEURESCUE APS, representing a 100% industry ratio. This lean structure suggests a highly focused commercial drive, utilizing EU funding to bridge the gap between a TRL 7 prototype and a full commercial launch.
Contact NEURESCUE APS in Denmark for partnership opportunities.
Talk to the team behind this work.
Contact us to explore licensing opportunities for the patented sensor system.