Taiwan FDA registration 0224bd5047150e4f34f655e40ca8bf8d
"Meiyi" biliary stent
TW: "美易" 膽道支架
Registration details
- Analysis ID
- 0224bd5047150e4f34f655e40ca8bf8d
- Customs Code
- DHA00601042001
Company information
- Manufacturer
- M.I. TECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CHINA HOSMED INTERNATIONAL INC.
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Oct 07, 2003
- Expiry Date
- Oct 07, 2013
- Cancellation Date
- Apr 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Meiyi" biliary stent in Taiwan's medical device market through Pure Global AI's free database. is registered under number 0224bd5047150e4f34f655e40ca8bf8d and manufactured by M.I. TECH CO., LTD.. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices