Coverage

Best Practice Guidance for UDI Compliance – published in Med-Tech Innovation

By Warren Stacey

The system means that by 2020 most medical devices will need to include a Unique Device Identifier (UDI) in human and machine-readable form. In addition, device labellers must submit mandatory data about each device to the FDA/National Library of Medicine’s Global Unique Device Identification Database (GUDID), enabling the public and healthcare stakeholders to access and download device information.

READ THE FULL ARTICLE HERE PAGE 24/25

 UDI article