Taiwan FDA registration f75bc7d3fd10cc681ffb68370044bbe9
"Taiwu" esophageal stent
TW: "泰悟" 食道支架
Taiwan·Risk Class 2·TAEWOONG MEDICAL CO., LTD.·Registered Jun 29, 2005 – Jun 29, 2020CancelledRegistration details
- Analysis ID
- f75bc7d3fd10cc681ffb68370044bbe9
- Customs Code
- DHA00601149409
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.3610 Esophageal complement
- Import Information
- import
Dates and status
- Registration Date
- Jun 29, 2005
- Expiry Date
- Jun 29, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Taiwu" esophageal stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f75bc7d3fd10cc681ffb68370044bbe9 and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is HOPE SING MEDICAL INSTRUMENTS CO., LTD..
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