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“Gyrus ACMI” Dual Lumen Catheter - Taiwan Registration fa7c727bc68229b49644735759550f81

Access comprehensive regulatory information for “Gyrus ACMI” Dual Lumen Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa7c727bc68229b49644735759550f81 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

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fa7c727bc68229b49644735759550f81
Registration Details
Taiwan FDA Registration: fa7c727bc68229b49644735759550f81
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Device Details

“Gyrus ACMI” Dual Lumen Catheter
TW: “吉洛氏 艾斯米”雙腔導管
Risk Class 2
MD

Registration Details

fa7c727bc68229b49644735759550f81

Ministry of Health Medical Device Import No. 027405

DHA05602740500

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H5130 Urinary catheters and their accessories

Imported from abroad

Dates and Status

May 28, 2015

May 28, 2025