"Gore" Predford pericardial replacement membrane - Taiwan Registration 42ae6b804a54e5d48c671f5a4287e344
Access comprehensive regulatory information for "Gore" Predford pericardial replacement membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42ae6b804a54e5d48c671f5a4287e344 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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42ae6b804a54e5d48c671f5a4287e344
Registration Details
Taiwan FDA Registration: 42ae6b804a54e5d48c671f5a4287e344
Device Details
"Gore" Predford pericardial replacement membrane
TW: "ๆ็พ"ๆฎ็ๅพ็ฆๅฟๅ
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Risk Class 2

