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
At the Medtech Europe, starting tomorrow in Stuttgart, FOBA will demonstrate laser marking on medical forceps. Visitors can get this trade show sample and see in live demonstrations, how vision-based automated laser positioning enables accurate marking results, even on products that are totally out of alignment from their expected positions.