On January 27, 2016, from 1:00 to 3:00 PM, Eastern Time, the Center for Devices and Radiological Health’s (CDRH) Division of Industry and Consumer Education (DICE) will host the first of two CDRH Industry Basics Workshops on Unique Device Identification (UDI).
- There is no fee to attend and registration is not required.
- Target Audience: Labelers of Class II devices, other than Implantable, Life-Supporting, and Life-Sustaining Devices
- For more information and instructions on how to attend, please see the CDRH Industry Basics webpage .
For questions about the Industry Basics series, please contact DICE@fda.hhs.gov.
For more information about the Unique Device Identification (UDI) System, please visit the FDA’s UDI webpage.
We plan to offer the second session of this UDI Industry Basics workshop in the spring of 2016 to explain how to submit data to the GUDID.