Taiwan FDA registration f22a63d1fd4f725609e820353d80b419
"Minimally invasive" disposable expansion balloons
TW: “微創”拋棄式擴張氣球
Taiwan·Risk Class 2·Micro-Tech (Nanjing) Co., Ltd.·Registered Feb 20, 2017 – Feb 20, 2027ActiveRegistration details
- Analysis ID
- f22a63d1fd4f725609e820353d80b419
- Customs Code
- DHA09200082100
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)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5365 Esophageal extenders
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Feb 20, 2017
- Expiry Date
- Feb 20, 2027
About this record
Access comprehensive regulatory information for "Minimally invasive" disposable expansion balloons in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f22a63d1fd4f725609e820353d80b419 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.
Free DatabasePowered by Pure Global AI89,000+ Devices