Category: Medical Devices

Booth #: S19.H118

Understanding and implementing Unique Device Identification (UDI) requirements can be one of the most complex challenges for medical device professionals. In this session, our labeling and regulatory experts will break down the logic behind medical device labeling and guide you through the most common pitfalls that can delay compliance or create costly errors.  Join us

Booth Number: Hall 6, D33

Nothing derails supply chains like FDA import detentions. This webinar will help you understand what triggers detentions, how Import Alerts work, and what steps you can take to keep your medical devices moving across borders without delays. Learn best practices for documentation, product coding, and how to respond if issues arise—all backed by real-world scenarios.

Perfect for newcomers and professionals seeking a refresher, this webinar provides a clear, practical introduction to the regulatory framework that governs medical devices in the United States. Learn how the FDA classifies devices, what pathways exist for market entry, and the compliance obligations every manufacturer must understand. 

Booth Number: Pending  

Booth Number: E12C25

Join us for an in-depth webinar designed for medical device manufacturers navigating FDA requirements related to product labeling, traceability, and Unique Device Identification (UDI). Whether you’re preparing your first UDI submission or reassessing your compliance program, this session offers a structured, strategic overview of what the FDA expects—and how to implement it correctly across your

As global trade dynamics continue to shift, customs brokers, international suppliers to the U.S., and importers must stay ahead of critical regulatory and policy changes that directly impact compliance and operations. From the evolving enforcement priorities at the U.S. Food and Drug Administration (FDA) to renewed scrutiny of de minimis thresholds and tariff policy under

Join Registrar Corp’s experts as they break down the fundamentals of medical device regulation in the United States. From device classification and 510(k) requirements to registration, labeling, and UDI compliance, this session is ideal for medical device companies looking to enter or expand in the U.S. market. #ExemptIsNotUnregulated

Booth #: Pending

Registrar Corp vi invita a partecipare al webinar “Requisiti FDA per i dispositivi medici negli USA “, organizzato in collaborazione con Ceipiemonte.

Booth Number: 15G12-8 in Hall 15