WebinarDemystifying UDI
Not sure what the U.S. FDA UDI Rule is or how it will impact your business?
Get a better understanding of class I requirements and what they mean for you.
Webinar DetailsHow the U.S. FDA UDI Rule impacts your business
With growing needs to identify medical devices to increase patient and consumer safety, the U.S. Food and Drug Administration (FDA) established the unique device identification (UDI) system to adequately identify medical devices sold in the United States from manufacturing through distribution to patient use.*
As deadlines for class I medical devices approach, do you know how this could impact your business? Retail products like bandages, electronic toothbrushes, tongue depressors or any other low-risk medical device can fall under this rule and will need to meet requirements.
- What is the U.S. FDA UDI Rule?Learn about the UDI Rule and upcoming deadlines
- Will this impact my business?Understand class I requirements and exceptions
- How do I get started?Learn about the GS1 Standards and tools that support the requirements, including sharing information to the Global Unique Device Identification Database (GUDID)
