FDA unique device identification system workshop (Feb. 12, 2009)

On February 12, 2009, the FDA is hosting a public workshop to obtain input on issued involved in the establishment of a unique device identification (UDI) system. The Food and Drug Administration Amendments Act of 2007 requires the establishment of a UDI system requiring the labeling of devices through distribution and use (subject to certain exceptions). The registration deadline for the workshop is January 30, 2009.