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“Endo-Upex” Biopsy Forceps - Taiwan Registration 6af1bbb876facfdb2608365737d314bb

Access comprehensive regulatory information for “Endo-Upex” Biopsy Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6af1bbb876facfdb2608365737d314bb and manufactured by UPEX-MED CO., LTD.. The authorized representative in Taiwan is MedPower Medical 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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6af1bbb876facfdb2608365737d314bb
Registration Details
Taiwan FDA Registration: 6af1bbb876facfdb2608365737d314bb
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Device Details

“Endo-Upex” Biopsy Forceps
TW: “安朵優倍斯”活體組織夾
Risk Class 2
MD

Registration Details

6af1bbb876facfdb2608365737d314bb

Ministry of Health Medical Device Import No. 035160

DHA05603516005

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H1075 Gastroenterology - Urology biopsy instruments

Imported from abroad

Dates and Status

Dec 30, 2021

Dec 30, 2026