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Medical device manufacturers selling products in Saudi Arabia must meet the Saudi Food and Drug Authority (SFDA) medical device and IVD UDI requirements.

Device manufacturers have very little time to put UDIs on their products and submit device data to the Saudi Arabia UDI Database (SAUDI-D). Watch this on-demand webinar to learn more about what you need to do to be ready.

The discussion included:

  • Details on compliance requirements
  • Overview of the Saudi Arabia UDI Database
  • Compliance deadlines based on device class
  • Q&A

About the Presenter

Jay Crowley
Jay Crowley

Vice President of Medical Device Solutions and Services Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for the FDA’s Unique Device Identification system.

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