EU Regulation 2024/1781: New Sustainability Requirements for Medical Devices

EU Regulation 2024/1781: New Sustainability Requirements for Medical Devices

ISEMED Channel is the dedicated space for updates, innovations, and regulatory insights in the fields of medical devices, IVDs, cosmetics, and biocides.

In this episode, Engineer Guido Bonapace, Founder & Senior Consultant at ISEMED Srl, walks us through the key updates introduced by EU Regulation 2024/1781, which establishes, for placing products on the European market:
🔹 Essential ecodesign requirements, aimed at redefining the concept of compliance and environmental responsibility;
🔹 The new Digital Product Passport, designed to ensure sustainability traceability throughout the entire lifecycle of the device.

A new paradigm for the medical device sector

With enforcement expected to begin in mid-2027, the regulation marks a true paradigm shift for the medical device industry, requiring a strategic review of product design processes.

Pegaso Management, in collaboration with its partner ISEMED, supports companies in adapting to the new regulatory framework and transitioning towards more sustainable production models, aligned with EU directives and ESG goals.

🎥 Watch the full video here: