UDI Reference Center
EUDAMED
Global UDI
GUDID
Try Global UDI Connector for 30 days at no cost!
Global UDI Reference Center
Global UDI Developments
There is ongoing uncertainty when it comes to Unique Device Identifcation (UDI) regulations and compliance timelines as each country’s regulator continues to change the scope of their UDI implementation. Despite the concerted efforts of International Medical Device Regulators Forum (IMDRF), divergence in UDI policy and strategy is adding complexity for medical device companies to comply with regulatory data submission mandates, especially those with multi-national operations. Fortunately, Innovit is here to to help you navigate these country-specific deadlines and UDI data requirements.
Global UDI Timelines
Your Critical Path to UDI key dates around the world.
Global UDI Map
Your Critical Path to UDI key dates around the world.
Featured Story
Top 12 Things to Prepare for Your UDI Journey
Manufacturers distributing products multi-nationally need to address the rapidly approaching global UDI requirements in play in the U.S. and Europe. But there are a number of other countries that are active, including China, South Korea, Saudi Arabia and more. In addition, there are several countries just beginning, or are in various stages of developing their UDI requirements.
Download our guide to learn the key steps for global UDI compliance.