HANAROSTENT® ESOPHAGUS SKIDPROOF (CCC)/ ECD - FDA Registration MDR-10080F

Access comprehensive regulatory information for HANAROSTENT® ESOPHAGUS SKIDPROOF (CCC)/ ECD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10080F and manufactured by M.I. Tech Co., Ltd. in Republic of Korea. The device was registered on July 24, 2020.

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.