Navigating the FDA's import regulations requires a clear understanding of two critical, yet distinct, roles: the U.S. Agent and the Initial Importer. This episode breaks down their specific responsibilities, explaining how confusing them can lead to costly customs delays and compliance failures. We explore the specific regulatory burdens of the Initial Importer, including Medical Device Reporting and device listing, and highlight why manufacturers must verify their distributor’s capabilities to ensure smooth market entry. • What is the fundamental difference between an FDA U.S. Agent and an Initial Importer? • Why is the U.S. Agent's role primarily administrative and not related to compliance? • What specific regulatory responsibilities, like MDR, does an Initial Importer handle? • How can selecting the wrong Initial Importer halt your device shipments at the border? • What are the most common errors in entry filings related to import roles? • How do you verify if your distributor is truly ready to act as your Initial Importer? • What post-market surveillance duties fall on the Initial Importer? Ready to turn these insights into your competitive edge? Pure Global’s regulatory experts guide MedTech companies through every step of 30+ markets worldwide. Explore how we can accelerate your market entry at https://pureglobal.com or email [email protected] for tailored support.