"Decant Flex" aortic stent system - Taiwan Registration 4c2567de5b42705c1716b107e6c80d5f
Access comprehensive regulatory information for "Decant Flex" aortic stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4c2567de5b42705c1716b107e6c80d5f and manufactured by Bentley InnoMed GmbH. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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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4c2567de5b42705c1716b107e6c80d5f
Registration Details
Taiwan FDA Registration: 4c2567de5b42705c1716b107e6c80d5f
Device Details
"Decant Flex" aortic stent system
TW: โๆฝท่็ฟๅญโไธปๅ่่ฆ่ๆฏๆถ็ณป็ตฑ
Risk Class 3

