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“GORE” MOLDING AND OCCLUSION BALLOON CATHETER - Taiwan Registration 2aa41bebd44bae098760cac77c3fcdc8

Access comprehensive regulatory information for “GORE” MOLDING AND OCCLUSION BALLOON CATHETER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2aa41bebd44bae098760cac77c3fcdc8 and manufactured by W.L. GORE & ASSOCIATES, INC.. The authorized representative in Taiwan is W.L. GORE & ASSOCIATES (HONG KONG) LTD. TAIWAN BRANCH (H.K.).

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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2aa41bebd44bae098760cac77c3fcdc8
Registration Details
Taiwan FDA Registration: 2aa41bebd44bae098760cac77c3fcdc8
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Device Details

“GORE” MOLDING AND OCCLUSION BALLOON CATHETER
TW: “戈爾”成型和阻塞球囊導管
Risk Class 2
MD

Registration Details

2aa41bebd44bae098760cac77c3fcdc8

Ministry of Health Medical Device Import No. 033569

DHA05603356903

Company Information

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Apr 20, 2020

Apr 20, 2025