HANAROSTENT® DUODENUM/PYLORUS LASSO (NNN) NDSL STENT - FDA Registration MDR-10105B
Access comprehensive regulatory information for HANAROSTENT® DUODENUM/PYLORUS LASSO (NNN) NDSL STENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10105B 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.
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Republic of Korea
MDR-10105B
HANAROSTENT® DUODENUM/PYLORUS LASSO (NNN) NDSL STENT
Registered medical device in Philippines
Device Information
Product Name
HANAROSTENT® DUODENUM/PYLORUS LASSO (NNN) NDSL STENT
Registration Number
MDR-10105B
Manufacturer Details
Manufacturer
M.I. Tech Co., Ltd.Country of Origin
Republic of Korea
Importer & Distribution
Importer/Distributor
Alfamed Care EnterpriseRegistration Dates
Issuance Date
July 30, 2020
Expiry Date
July 30, 2021

