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“Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length Ureteral Stents - Taiwan Registration 0b94f1da941d9f5eb2ba968d1383fafd

Access comprehensive regulatory information for “Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length 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 0b94f1da941d9f5eb2ba968d1383fafd and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

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0b94f1da941d9f5eb2ba968d1383fafd
Registration Details
Taiwan FDA Registration: 0b94f1da941d9f5eb2ba968d1383fafd
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Device Details

“Gyrus ACMI” Tecoflex Quadra-Coil Multi-Length Ureteral Stents
TW: “吉洛氏 艾斯米”泰柯弗立士可達輸尿管支架
Risk Class 2
MD

Registration Details

0b94f1da941d9f5eb2ba968d1383fafd

Ministry of Health Medical Device Import No. 028050

DHA05602805007

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

Jan 15, 2016

Jan 15, 2026