Direct Part Marking (DPM) Applications • Medical Device and Implants / Typically laser etch or dot peen є FDA UDI for Class 2 reprocessed (reusable) devices with DPM, Sept. 2018 ‒ GS1 Table 7 defines marking requirements; GS1 DataMatrix or GS1 QR є EU Medical Device Regulations (MDR) and UK NHS UDI Compliance ‒ Sept 2019 for UK NHS Class 3 DPM devices in UK, 2022 for MDR є See Microscan,com/Resources whitepapers for further information • “Traditional” Markets є Automotive є Aerospace/Defense є Electronics • Emerging/New; QR DPM for food packaging