The Saudi Food and Drug Authority (SFDA) has released its “Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices” designating HIBCC as an Issuing Entity. The initial release date was April 8th, 2019.
To view the full guidance document click here.
To learn more about UDI contact HIBCC at firstname.lastname@example.org
- 17 Sep 2019HIBCC UDI Presentation Available for Download
- 27 Aug 2019European Commission releases FAQ for Unique Device Identification System (UDI)
- 26 Aug 2019HIBCC Upcoming Speaking Engagements
- 23 Aug 2019HIN User Account Page Enhanced to Provide Multiple Customer Identifiers
- 16 Aug 2019HIBCC establishes EU-MDR mailbox