Taiwan FDA registration 5672251ad4aa948a22eedb5bac8f43b5
“Taewoong” Pyloric/Duodenal Stent
TW: “泰悟”幽門/十二指腸支架
Taiwan·Risk Class 2·MD·TAEWOONG MEDICAL CO., LTD.·Registered Jul 06, 2018 – Jul 06, 2028ActiveRegistration details
- Analysis ID
- 5672251ad4aa948a22eedb5bac8f43b5
- License Form
- Ministry of Health Medical Device Import No. 031287
- Customs Code
- DHA05603128709
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)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3610 Esophageal supplements
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 06, 2018
- Expiry Date
- Jul 06, 2028
About this record
Access comprehensive regulatory information for “Taewoong” Pyloric/Duodenal Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5672251ad4aa948a22eedb5bac8f43b5 and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is HOPE SING MEDICAL INSTRUMENTS CO., LTD..
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