The healthcare sector is a large contributor to climate change, due to their size, resource use and extensive use of single-use devices (SUDs). Despite the European Medical Device Regulation (MDR) permitting the resetting of SUDs, healthcare professionals are hesitant and seek evidence-based guidelines. This demonstration study investigates how design engineering can contribute to the feasibility of resetting SUDs that are theoretically suitable for reuse, contributing to the broader discussion on medical device sustainability. The research focuses on the quality evalualtion of reset SUDs through a detailed protocol ensuring that reused devices meet safety and performance standards. Results reveal a discrepancy between the theoretical feasibility of resetting SUD and its actual practicability. This finding highlights the necessity for more practically oriented protocols.
