Taiwan FDA registration 29816618bf75a900201b20f0d03cbdbb

"Gore" trilobar balloon catheter

TW: “戈爾”三葉球囊導管

Taiwan·Risk Class 2·W.L. GORE & ASSOCIATES INC.·Registered Apr 13, 2010 – Apr 13, 2025Expired

Registration details

Analysis ID: 29816618bf75a900201b20f0d03cbdbb
Customs Code: DHA00602091001

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, such as changes in the efficacy, use or indications of the Chinese approved copy of the copy: Details such as the approved Chinese instructions (the original label, instruction manual or packaging approved on April 1, 109 shall be withdrawn and invalidated).
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.1250 Percutaneous catheters
Import Information: import

Dates and status

Registration Date: Apr 13, 2010
Expiry Date: Apr 13, 2025

About this record

Access comprehensive regulatory information for "Gore" trilobar 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 29816618bf75a900201b20f0d03cbdbb 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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