Taiwan FDA registration 063071ad3ab8331b335a5fa8a8c0ec4e
"Taiwu" tracheobronchial stent
TW: “泰悟”氣管支氣管支架
Taiwan·Risk Class 2·TAEWOONG MEDICAL CO., LTD.·Registered Sep 21, 2012 – Sep 21, 2027ActiveRegistration details
- Analysis ID
- 063071ad3ab8331b335a5fa8a8c0ec4e
- Customs Code
- DHA00602404106
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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3720 Gas Pipe Supplements
- Import Information
- import
Dates and status
- Registration Date
- Sep 21, 2012
- Expiry Date
- Sep 21, 2027
About this record
Access comprehensive regulatory information for "Taiwu" tracheobronchial stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 063071ad3ab8331b335a5fa8a8c0ec4e and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is HOPE SING MEDICAL INSTRUMENTS CO., LTD..
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