---
title: Unique Device Identifiers and the Global Unique Identifier Database
description: 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 in this downloadable guide.
image: https://www.thefdagroup.com/hubfs/Images/Covers/fda-Cover-UniqueDeviceIdentifiers-01.jpg
---

| ![](https://www.thefdagroup.com/hubfs/Images/Covers/fda-Cover-UniqueDeviceIdentifiers-01.jpg) | Get our free guide # 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 [Get my free guide »](https://www.thefdagroup.com/unique-device-identifiers-and-the-global-unique-identifier-database#) |
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