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"Gore" trilobar balloon catheter - Taiwan Registration 29816618bf75a900201b20f0d03cbdbb

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.).

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.

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29816618bf75a900201b20f0d03cbdbb
Registration Details
Taiwan FDA Registration: 29816618bf75a900201b20f0d03cbdbb
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Device Details

"Gore" trilobar balloon catheter
TW: โ€œๆˆˆ็ˆพโ€ไธ‰่‘‰็ƒๅ›ŠๅฐŽ็ฎก
Risk Class 2

Registration Details

29816618bf75a900201b20f0d03cbdbb

DHA00602091001

Company Information

Product Details

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approved Chinese instructions (the original label, instruction manual or packaging approved on April 1, 109 shall be withdrawn and invalidated).

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Apr 13, 2010

Apr 13, 2025