Pure Global

HANAROSTENT® DUODENUM/PYLORUS (NNN) NDS STENT - FDA Registration MDR-10105A

Access comprehensive regulatory information for HANAROSTENT® DUODENUM/PYLORUS (NNN) NDS STENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10105A and manufactured by M.I. Tech Co., Ltd. in Republic of Korea. The device was registered on July 30, 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.

Free Database
Powered by Pure Global AI
FDA Official Data
Republic of Korea
MDR-10105A
HANAROSTENT® DUODENUM/PYLORUS (NNN) NDS STENT
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Information
Product Name
HANAROSTENT® DUODENUM/PYLORUS (NNN) NDS STENT
Registration Number
MDR-10105A
Manufacturer Details
Country of Origin
Republic of Korea
Importer & Distribution
Importer/Distributor
Alfamed Care Enterprise
Registration Dates
Issuance Date
July 30, 2020
Expiry Date
July 30, 2021