Philippines FDA registration CMDR-2022-00554

Hanarostent® Plumber™ Biliary (CCC) Stent

Name: Hanarostent® Plumber™ Biliary (CCC) Stent — Philippines FDA registration CMDR-2022-00554
Creator: M.I. Tech Co., Ltd. 174 Habuk 2-gil, Jinwi-myeon, Pyeontaek-si, Gyeonggi-do, 17706, South Korea
Keywords: Hanarostent® Plumber™ Biliary (CCC) Stent, CMDR-2022-00554, M.I. Tech Co., Ltd. 174 Habuk 2-gil, Jinwi-myeon, Pyeontaek-si, Gyeonggi-do, 17706, South Korea, Alfamed Care Enterprise, South Korea, Philippines FDA registration

PhilippinesM.I. Tech Co., Ltd. 174 Habuk 2-gil, Jinwi-myeon, Pyeontaek-si, Gyeonggi-do, 17706, South KoreaSouth KoreaIssued November 15, 2022 – April 29, 2027

VerifiedFDA Philippines · official registry

Device information

Product Name: Hanarostent® Plumber™ Biliary (CCC) Stent
Registration Number: CMDR-2022-00554

Manufacturer details

Manufacturer: M.I. Tech Co., Ltd. 174 Habuk 2-gil, Jinwi-myeon, Pyeontaek-si, Gyeonggi-do, 17706, South Korea
Country of Origin: South Korea

Importer & distribution

Importer/Distributor: Alfamed Care Enterprise

Registration dates

Issuance Date: November 15, 2022
Expiry Date: April 29, 2027

About this record

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.