Taiwan FDA registration 06584f4471556ba851d5f130de9e324b
“Micro-Tech” Tracheal/Bronchial Stent
TW: “微創”氣管支氣管支架
Taiwan·Risk Class 2·MD·Micro-Tech (Nanjing) Co., Ltd.·Registered Mar 28, 2020 – Mar 28, 2025ExpiredRegistration details
- Analysis ID
- 06584f4471556ba851d5f130de9e324b
- License Form
- Ministry of Health Medical Device Land Transport No. 001120
- Customs Code
- DHA09200112001
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 and plastic surgical devices
- Product Type (Level 2)
- I3720 Tracheal Supplement
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Mar 28, 2020
- Expiry Date
- Mar 28, 2025
About this record
Access comprehensive regulatory information for “Micro-Tech” Tracheal/Bronchial Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06584f4471556ba851d5f130de9e324b and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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