The document summarizes an upcoming webinar about Unique Device Identification (UDI) rules and requirements for medical device industries, hospitals, and providers. The webinar will cover current and upcoming FDA UDI policies, including timelines and guidance documents. It will explain UDI codes and standards, requirements for different industry roles, and how organizations should prepare to comply with increasing regulatory complexity around medical device identification and post-market surveillance. The webinar aims to help participants from various medical device and healthcare roles understand and conform to evolving UDI regulations.