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"Gore" Will rod peripheral vascular stents - Taiwan Registration 0a1c644d23583fb7d06035805ae0480f

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.).

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0a1c644d23583fb7d06035805ae0480f
Registration Details
Taiwan FDA Registration: 0a1c644d23583fb7d06035805ae0480f
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Device Details

"Gore" Will rod peripheral vascular stents
TW: โ€œๆˆˆ็ˆพโ€ๅจ็ˆพๆฃ’ๅ‘จ้‚Š่ก€็ฎกๆ”ฏๆžถ
Risk Class 3

Registration Details

0a1c644d23583fb7d06035805ae0480f

DHA00601958908

Company Information

Product Details

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.

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

Nov 18, 2008

Nov 18, 2023