Taiwan FDA registration 2a92eefca56afc3ea96257ea56ddd54a
“Gyrus ACMI” Tecoflex Classic Double PigTail Ureteral Stents (Uncoated)
TW: “吉洛氏 艾斯米”泰柯弗立士雙豬尾型輸尿管支架(無塗層)
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered May 01, 2015 – May 01, 2025ExpiredRegistration details
- Analysis ID
- 2a92eefca56afc3ea96257ea56ddd54a
- License Form
- Ministry of Health Medical Device Import No. 027376
- Customs Code
- DHA05602737606
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
- May 01, 2015
- Expiry Date
- May 01, 2025
About this record
Access comprehensive regulatory information for “Gyrus ACMI” Tecoflex Classic Double PigTail Ureteral Stents (Uncoated) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a92eefca56afc3ea96257ea56ddd54a and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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