Taiwan FDA registration bfd49769387a921fcf91dcfd6480b852
"Minimally invasive" tracheobronchial stents
TW: “微創”氣管支氣管支架
Registration details
- Analysis ID
- bfd49769387a921fcf91dcfd6480b852
- Customs Code
- DHA09200112001
Company information
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- AP Biotech 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
- Mar 28, 2020
- Expiry Date
- Mar 28, 2025
About this record
Access comprehensive regulatory information for "Minimally invasive" tracheobronchial stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bfd49769387a921fcf91dcfd6480b852 and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is AP Biotech Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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