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“Applied” Kii Dissecting Balloon Access System - Taiwan Registration 8971714ff1a42bc8a144076f1fe7e2f6

Access comprehensive regulatory information for “Applied” Kii Dissecting Balloon Access System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8971714ff1a42bc8a144076f1fe7e2f6 and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..

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8971714ff1a42bc8a144076f1fe7e2f6
Registration Details
Taiwan FDA Registration: 8971714ff1a42bc8a144076f1fe7e2f6
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Device Details

“Applied” Kii Dissecting Balloon Access System
TW: “安培”腹腔鏡氣球撐開式套管
Risk Class 2
MD

Registration Details

8971714ff1a42bc8a144076f1fe7e2f6

Ministry of Health Medical Device Import No. 034135

DHA05603413501

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Dec 25, 2020

Dec 25, 2025