Taiwan FDA registration 0b94f1da941d9f5eb2ba968d1383fafd
“Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length Ureteral Stents
TW: “吉洛氏 艾斯米”泰柯弗立士可達輸尿管支架
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered Jan 15, 2016 – Jan 15, 2026ExpiredRegistration details
- Analysis ID
- 0b94f1da941d9f5eb2ba968d1383fafd
- License Form
- Ministry of Health Medical Device Import No. 028050
- Customs Code
- DHA05602805007
Company information
- Manufacturer
- Gyrus ACMI, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H4620 Ureteral stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 15, 2016
- Expiry Date
- Jan 15, 2026
About this record
Access comprehensive regulatory information for “Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length Ureteral Stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b94f1da941d9f5eb2ba968d1383fafd and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT 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