Since the Food & Drug Administration (FDA) announced the upcoming implementation of obligatory Unique Device Identification (UDI) marking for medical devices, manufacturers have been searching for feasible and economic marking solutions. Read More
Following the Unique Device Identification directive (UDI), mandated by the Food & Drug Administration (FDA), medical devices have to be clearly identified to ensure traceability and patient safety. The rule-compliant implementation challenges medical device manufacturers and raises many questions. Read More
Well, you might expect from a person with my background that there is only one possible answer. However, I believe that the appropriate answer is: It really depends.