Taiwan FDA registration c78dac9ae0e26c2002777d1b716d625c

"Gore" readily fixed a stent for abdominal aortic aneurysm

TW: “戈爾”易時固得腹主動脈瘤支架

Taiwan·Risk Class 3·W.L. GORE & ASSOCIATES, INC.·Registered Apr 24, 2008 – Apr 24, 2028Active

Registration details

Analysis ID: c78dac9ae0e26c2002777d1b716d625c
Customs Code: DHA00601901804

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: For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.0001 Cardiovascular stents
Import Information: import

Dates and status

Registration Date: Apr 24, 2008
Expiry Date: Apr 24, 2028

About this record

Access comprehensive regulatory information for "Gore" readily fixed a stent for abdominal aortic aneurysm in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c78dac9ae0e26c2002777d1b716d625c 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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