Taiwan FDA registration 2492a60eea8688ebdeba404cda0bff1d
“Gyrus ACMI” LithoStent Ureteral Stents
TW: “吉洛氏 艾斯米”李瑟輸尿管支架
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered May 25, 2015 – May 25, 2025ExpiredRegistration details
- Analysis ID
- 2492a60eea8688ebdeba404cda0bff1d
- License Form
- Ministry of Health Medical Device Import No. 027396
- Customs Code
- DHA05602739602
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 25, 2015
- Expiry Date
- May 25, 2025
About this record
Access comprehensive regulatory information for “Gyrus ACMI” LithoStent 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 2492a60eea8688ebdeba404cda0bff1d and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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