Taiwan FDA registration 9395cbe5b4c2d3ac9fbc00647703e477
“Gyrus ACMI” Silicone Single-J Urinary Diversion Stent
TW: “吉洛氏 艾斯米”矽力控單彎型尿流改道支架
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered May 12, 2015 – May 12, 2025ExpiredRegistration details
- Analysis ID
- 9395cbe5b4c2d3ac9fbc00647703e477
- License Form
- Ministry of Health Medical Device Import No. 027383
- Customs Code
- DHA05602738303
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 12, 2015
- Expiry Date
- May 12, 2025
About this record
Access comprehensive regulatory information for “Gyrus ACMI” Silicone Single-J Urinary Diversion Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9395cbe5b4c2d3ac9fbc00647703e477 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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