Taiwan FDA registration 4a4ac57240efab789cf6d1688f1d2c6e
"Minimally invasive" tracheal stents
TW: “微創”氣管支架
Taiwan·Risk Class 2·Micro-Tech (Nanjing) Co., Ltd.·Registered Nov 23, 2017 – Nov 23, 2022CancelledRegistration details
- Analysis ID
- 4a4ac57240efab789cf6d1688f1d2c6e
- Customs Code
- DHA09200090401
Company information
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- ERA BIOTEQ ENTERPRISE 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Nov 23, 2017
- Expiry Date
- Nov 23, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Minimally invasive" tracheal stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a4ac57240efab789cf6d1688f1d2c6e and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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