Hanarostent® Plumber™ Biliary (CCC) Stent - FDA Registration CMDR-2022-00554

Access comprehensive regulatory information for Hanarostent® Plumber™ Biliary (CCC) Stent in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00554 and manufactured by M.I. Tech Co., Ltd. 174 Habuk 2-gil, Jinwi-myeon, Pyeontaek-si, Gyeonggi-do, 17706, South Korea in South Korea. The device was registered on November 15, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Alfamed Care Enterprise), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.