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“Gore” VIABAHN Endoprosthesis with Heparin Bioactive Surface - Taiwan Registration 4550f1165f7353f53556289ed4e323ec

Access comprehensive regulatory information for “Gore” VIABAHN Endoprosthesis with Heparin Bioactive Surface in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4550f1165f7353f53556289ed4e323ec 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.).

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4550f1165f7353f53556289ed4e323ec
Registration Details
Taiwan FDA Registration: 4550f1165f7353f53556289ed4e323ec
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Device Details

“Gore” VIABAHN Endoprosthesis with Heparin Bioactive Surface
TW: “戈爾”威爾棒周邊血管支架
Risk Class 2
MD

Registration Details

4550f1165f7353f53556289ed4e323ec

Ministry of Health Medical Device Import No. 031607

DHA05603160701

Company Information

Product Details

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

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Mar 08, 2019

Mar 08, 2024