French medical technology company Carmat has launched a new software enhancement for its artificial heart Aeson.
The enhancement is claimed to have been designed to significantly improve Aeson’s safety profile.
Go deeper with GlobalData
Discover B2B Marketing That Performs
Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.
With this update, the prosthesis software can be enabled to detect potential malfunctions in real time and adjust its control accordingly for uninterrupted patient support.
Carmat’s research teams have developed and tested these changes. The software enhancement will initially be rolled out to all hearts currently implanted in patients.
This will be done through a software update, accompanied by the publication of a field safety notice.
Following this, the enhanced software will be integrated into the Aeson production process, pending necessary regulatory approvals.
US Tariffs are shifting - will you react or anticipate?
Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.
By GlobalDataThe implementation of this software modification complies with regulations. The rollout of the updated software will begin in the next few days.
Carmat CEO Stéphane Piat said: “In all industries, electronic components are potentially subject to failure because perfection of their manufacturing is almost impossible to achieve.
“It was important to be able to manage such risks in the case of our device, and I’m therefore very proud of the feat achieved by our software engineers: from now on, for many of the potential malfunctions linked to the prosthesis’s electronic components, Aeson software will automatically ‘correct’ these faults by adapting the prosthesis’s performance in an appropriate manner, so that the patient’s support remains unaffected.”
Piat added: “For me, this is a major and immediate step forward for all the patients who benefit and will benefit from our therapy; but also in the long term, when it comes to obtaining the destination therapy indication for Aeson, as this improvement significantly strengthens the safety profile and therefore the potential durability of the prosthesis.”
Last month, the artificial organ developer opened a new production facility in Bois-d’Arcy, France. It is its second facility which will be in the same vicinity as its first operations site.
