Taiwan FDA registration 0a1c644d23583fb7d06035805ae0480f

"Gore" Will rod peripheral vascular stents

TW: “戈爾”威爾棒周邊血管支架

Taiwan·Risk Class 3·W.L. GORE & ASSOCIATES INC.·Registered Nov 18, 2008 – Nov 18, 2023Expired

Registration details

Analysis ID: 0a1c644d23583fb7d06035805ae0480f
Customs Code: DHA00601958908

Company information

Manufacturer: W.L. GORE & ASSOCIATES INC.
Manufacturer Country: United States
Authorized Representative: W.L. GORE & ASSOCIATES (HONG KONG) LTD. TAIWAN BRANCH (H.K.)

Product details

Intended Use: It is used to improve the peripheral blood vessels of the superficial femoral artery of patients, and the vascular function damage with a caliber of 4.0~7.5mm to improve vascular embolism and promote blood flow.
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.0001 Cardiovascular stents
Import Information: import

Dates and status

Registration Date: Nov 18, 2008
Expiry Date: Nov 18, 2023

About this record

Access comprehensive regulatory information for "Gore" Will rod peripheral vascular stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0a1c644d23583fb7d06035805ae0480f 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.