FDA Rule for Unique Device Identification System The Food and Drug Administration (FDA) issued a final rule on October 24, 2013 to establish an identification

The U.S. Food and Drug Administration issued a long-awaited rule on Friday requiring companies to include Unique Device Identifiers, or UDIs, on medical devices. Each

July 3, 2012. In response to requirements in legislation that passed Congress with broad bipartisan support, the U.S. Food and Drug Administration proposed that most