On July 22, the FDA posted its final guidance regarding Global Unique Device Identification Database (GUDID) submission requirements for certain Class I devices considered consumer health products.
The FDA will enforce the GUDID submission requirements for Class I and unclassified devices, other than implantable, life-supporting or life-sustaining devices, regardless of whether they are consumer health products, on December 8, 2022.
If you’re a bit behind, there’s still time to ‘make this date’ and Innovit is here to help!
Join us for a webinar ‘9-Steps to GUDID Class I Medical Device Compliance’ on Tuesday, October 18, 2022 @ 7:30 AM PST.
Join our webinar to get a clear and concise process to comply to the FDA GUDID (database). In this webinar, you will learn:
- UDI definition and goals
- FDA UDI requirements & Class I exceptions
- The importance of label standardisation
- Nine easy steps to comply with the FDA’s GUDID compliance submission and maintenance
- How Innovit can help with your compliance journey