Taiwan FDA registration 19a47082c3a5d152c5bef334fa9763f8
“Gyrus ACMI” Tecoflex Ureteral Stents
TW: “吉洛氏 艾斯米”泰柯弗立士輸尿管支架
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered Oct 19, 2015 – Oct 19, 2025ExpiredRegistration details
- Analysis ID
- 19a47082c3a5d152c5bef334fa9763f8
- License Form
- Ministry of Health Medical Device Import No. 027823
- Customs Code
- DHA05602782305
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
- Oct 19, 2015
- Expiry Date
- Oct 19, 2025
About this record
Access comprehensive regulatory information for “Gyrus ACMI” Tecoflex 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 19a47082c3a5d152c5bef334fa9763f8 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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