This episode delves into the crucial role of the Pemegang Izin Edar, or Local Authorized Representative, for medical device market access in Indonesia. We explore the regulatory requirements mandated by the Ministry of Health, the responsibilities of the license holder, and the critical strategic differences between appointing a distributor versus an independent third party to hold your product registration. Understanding this choice is fundamental to maintaining control and flexibility in this key Southeast Asian market. Key Questions: • What is a "Pemegang Izin Edar" and why is it mandatory for foreign manufacturers in Indonesia? • Who is legally responsible for a medical device on the Indonesian market? • What are the main responsibilities of a Local Authorized Representative? • Should you appoint your distributor as your product license holder? • What are the risks of tying your device registration to a single commercial partner? • How can an independent license holder provide greater market flexibility and control? • What happens if you need to change your local representative in Indonesia? • Which key regulation, established in 2017, governs medical device distribution licenses? 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.