News
Visu selected by a leading Medical Device Manufacturer for Global UDI Compliance
06 Nov 2025: A major global medical device company has chosen DDi’s Visu platform to strengthen and streamline its Unique Device Identification (UDI) compliance processes across international markets as well as EUDAMED.
The selection comes as regulatory compliance expectations for device traceability continue to expand across regions, requiring manufacturers to maintain accurate product data, ensure timely submissions, and manage ongoing updates across multiple health authority systems.
Visu, DDi’s regulatory and quality data management and operations platform, centralizes UDI data, automates validation checks, and simplifies submissions to global databases including the FDA GUDID and EU EUDAMED.
With this deployment, the medical device maker aims to accelerate UDI readiness, enhance product data consistency, and reduce manual effort across regulatory and quality teams. The platform’s configurable workflows, audit-ready traceability, and integration capabilities were key factors in the selection.
This collaboration highlights the increasing adoption of advanced data and automation-driven solutions to meet evolving regulatory compliance demands while ensuring patient safety and product transparency.
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