1. Registration additions can be made in the following cases: (1) Adding product categories (2) Adding products |
Processing Time : 30 Working Days Required Documents : 1. Registration license from BKPM (Investment Coordinating Board) 2. Building floor plan 3. List of types of medical devices to be distributed 4. Medical device brochures or catalogs (if available) 5. Inventory of warehouse facilities and infrastructure 6. Workshop equipment (specifically for distributing electronic medical devices and/or in vitro diagnostic products) 7. After-sales warranty statement (specifically for distributing electronic medical devices and/or in vitro diagnostic products) 8. List of technicians’ names (specifically for distributing electronic medical devices and/or in vitro diagnostic products) 9. Copies of technicians’ diplomas (specifically for distributing electronic medical devices and/or in vitro diagnostic products) 10. Radiation Protection Officer (specifically for distributing electronic medical devices and/or in vitro diagnostic products) 11. Previous IDAK distributor license 12. Distribution report |