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“Gyrus ACMI” Silicone Double-J, Tractfinder, and Classic Closed Tip Ureteral Stents - Taiwan Registration 483008e9eaa5623ab376f64064d8ce67

Access comprehensive regulatory information for “Gyrus ACMI” Silicone Double-J, Tractfinder, and Classic Closed Tip 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 483008e9eaa5623ab376f64064d8ce67 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

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483008e9eaa5623ab376f64064d8ce67
Registration Details
Taiwan FDA Registration: 483008e9eaa5623ab376f64064d8ce67
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Device Details

“Gyrus ACMI” Silicone Double-J, Tractfinder, and Classic Closed Tip Ureteral Stents
TW: “吉洛氏 艾斯米”矽力控雙彎型輸尿管支架
Risk Class 2
MD

Registration Details

483008e9eaa5623ab376f64064d8ce67

Ministry of Health Medical Device Import No. 027385

DHA05602738507

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 12, 2015

May 12, 2025