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“Gyrus ACMI” Tecoflex Classic Double PigTail Ureteral Stents (Uncoated) - Taiwan Registration 2a92eefca56afc3ea96257ea56ddd54a

Access comprehensive regulatory information for “Gyrus ACMI” Tecoflex Classic Double PigTail Ureteral Stents (Uncoated) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a92eefca56afc3ea96257ea56ddd54a and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2a92eefca56afc3ea96257ea56ddd54a
Registration Details
Taiwan FDA Registration: 2a92eefca56afc3ea96257ea56ddd54a
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Device Details

“Gyrus ACMI” Tecoflex Classic Double PigTail Ureteral Stents (Uncoated)
TW: “吉洛氏 艾斯米”泰柯弗立士雙豬尾型輸尿管支架(無塗層)
Risk Class 2
MD

Registration Details

2a92eefca56afc3ea96257ea56ddd54a

Ministry of Health Medical Device Import No. 027376

DHA05602737606

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 01, 2015

May 01, 2025