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Unique Device Identifiers and the Global Unique Identifier Database

Understanding new UDI regulations and how to comply with them

Since 2013, medical device manufacturers have been required to enter unique device identifiers (UDIs) for each of their products into a national database to address issues with supply chains, reporting of adverse events, recalls, and more.

We’ve summarized the key UDI requirements all device manufacturers need to follow, as well as a step-by-step guide to implementing UDIs into your production process.

What you'll find inside:

• The basic features of UDIs and the national UDI database
• A simple guide to implementing UDI deployment into your current quality system
• What device manufacturer executives need to know about the current UDI requirements