9-Steps to GUDID Class I Medical Device Compliance

by Innovit Corporate Affairs | October 11, 2022 | Blog

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 standardization
  • Nine easy steps to comply with the FDA’s GUDID compliance submission and maintenance
  • How Innovit can help with your compliance journey
  • Q&A