Hanarostent® Colon/rectum Stent (NNN) - FDA Registration CDMR-2022-00605A

Access comprehensive regulatory information for Hanarostent® Colon/rectum Stent (NNN) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CDMR-2022-00605A and manufactured by M.I. Tech Co., Ltd Habuk 2-gil, Jinwi-myeon, Pyeongtaek-si, Gyeonggi-do, 17706, Korea in Korea. The device was registered on June 10, 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.