Taiwan FDA registration eb52cf9a384bb4a98b24611443fb45b2
“Taewoong” Biliary Stent
TW: “泰悟”膽道支架
Taiwan·Risk Class 2·MD·TAEWOONG MEDICAL CO., LTD.·Registered Oct 11, 2017 – Oct 11, 2027ActiveRegistration details
- Analysis ID
- eb52cf9a384bb4a98b24611443fb45b2
- License Form
- Ministry of Health Medical Device Import No. 030330
- Customs Code
- DHA05603033005
Company information
- Manufacturer
- TAEWOONG MEDICAL CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HOPE SING MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5010 Bile ductal catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 11, 2017
- Expiry Date
- Oct 11, 2027
About this record
Access comprehensive regulatory information for “Taewoong” Biliary Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eb52cf9a384bb4a98b24611443fb45b2 and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is HOPE SING MEDICAL INSTRUMENTS CO., LTD..
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