Brazil's INMETRO Certification: A Guide for Korean Electro-Medical Device Manufacturers

This episode focuses on a critical regulatory hurdle for Korean medical device companies entering the Brazilian market: the mandatory INMETRO certification for electro-medical devices. We break down why this certification, which requires local testing in Brazil, is often an unexpected challenge for manufacturers accustomed to the MFDS system. We cover the specific devices affected, the typical timelines of three to twelve months, and the ongoing costs associated with maintenance audits, providing a clear overview of this significant market access barrier. Key Questions: - What is INMETRO certification and why is it mandatory for certain medical devices in Brazil? - How does Brazil's local testing requirement differ from the process recognized by Korea's MFDS? - Which international standard, IEC 60601, triggers the need for INMETRO certification? - What is the expected timeline for achieving this certification, from start to finish? - Are there ongoing costs and audits required to maintain INMETRO certification after approval? - Why must Korean companies budget for this as a separate, significant market access expense? Pure Global offers end-to-end regulatory consulting for MedTech and IVD companies, streamlining global market access with local expertise and advanced AI. Whether you're navigating Brazil's INMETRO certification or entering any of our 30+ markets, our team provides comprehensive support from regulatory strategy and technical dossier submission to post-market surveillance. We act as your local representative, ensuring a smooth path to market. To accelerate your global expansion and leverage our powerful AI and data tools, contact us at [e-mail], visit https://pureglobal.com, or explore our free resources at https://pureglobal.ai.