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“Gyrus ACMI” LithoStent Ureteral Stents - Taiwan Registration 2492a60eea8688ebdeba404cda0bff1d

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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2492a60eea8688ebdeba404cda0bff1d
Registration Details
Taiwan FDA Registration: 2492a60eea8688ebdeba404cda0bff1d
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Device Details

“Gyrus ACMI” LithoStent Ureteral Stents
TW: “吉洛氏 艾斯米”李瑟輸尿管支架
Risk Class 2
MD

Registration Details

2492a60eea8688ebdeba404cda0bff1d

Ministry of Health Medical Device Import No. 027396

DHA05602739602

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H4620 Ureteral stents

Imported from abroad

Dates and Status

May 25, 2015

May 25, 2025