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This webinar will walk you through the full scope of the FDA’s Unique Device Identification (UDI) requirements and the Global Unique Device Identification Database (GUDID) — essential for medical device traceability, labeling compliance, and audit readiness. Whether you're preparing your first UDI submission or correcting legacy records, this session will help you understand your obligations under 21 CFR Parts 801 and 830 and avoid costly regulatory missteps.

Engage with our regulatory experts in a live Q&A to address your most important compliance questions.

0:00 Introductions
1:09 Introduction – Registrar Corp, FDA & Medical Device Definition
4:04 Unique Device Identifier – UDI
35:13 Global Unique Device Identifier Database – GUDID
57:32 Alternatives, Exceptions and Exemptions
1:13:26 UDI Worldwide
1:15:51 Registrar Corp Service
1:17:31 Q&A