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“Gyrus ACMI” Tecoflex Ureteral Stents - Taiwan Registration 19a47082c3a5d152c5bef334fa9763f8

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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19a47082c3a5d152c5bef334fa9763f8
Registration Details
Taiwan FDA Registration: 19a47082c3a5d152c5bef334fa9763f8
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Device Details

“Gyrus ACMI” Tecoflex Ureteral Stents
TW: “吉洛氏 艾斯米”泰柯弗立士輸尿管支架
Risk Class 2
MD

Registration Details

19a47082c3a5d152c5bef334fa9763f8

Ministry of Health Medical Device Import No. 027823

DHA05602782305

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

Oct 19, 2015

Oct 19, 2025