Skip to main content
blog_bg

Whitepaper

FDA UDI Vs EU UDI

Unique Device Identification (UDI) is intended to assign a unique identifier to medical devices within the United States it marks and identifies individual medical devices throughout their distribution and product life. The UDI system was initially created, developed, and maintained by the device manufacturer based on global device identification standards. Today, it also helps with procurement and reimbursement

FDA-UDI-Vs-EU-UDI

    The First Step

    Let's talk about how DDi can help you