This episode demystifies Argentina's medical device registration process under the national regulatory body, ANMAT. We provide a detailed breakdown of the essential framework established by Disposition 9688 of 2019, covering everything from risk classification and registration pathways to the critical requirements for foreign manufacturers seeking market entry. Key Questions: • What is ANMAT Disposition 9688/2019 and why is it essential for MedTech manufacturers? • How does Argentina classify medical devices based on risk? • What are the different registration pathways for Class I, II, III, and IV devices? • Is it mandatory to appoint an Argentina Authorized Representative (AAR)? • What are the Spanish language requirements for technical documentation? • How long is a medical device registration valid in Argentina? • Can an MDSAP certificate simplify my quality system compliance with ANMAT? • What are the Good Manufacturing Practice (GMP) requirements for Argentina? 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.