"Udek" Ines multi-branch stent graft system - Taiwan Registration 30194d597bbc8669f1f22fa1fced1e9a
Access comprehensive regulatory information for "Udek" Ines multi-branch stent graft system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 30194d597bbc8669f1f22fa1fced1e9a and manufactured by Jotec GmbH. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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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30194d597bbc8669f1f22fa1fced1e9a
Registration Details
Taiwan FDA Registration: 30194d597bbc8669f1f22fa1fced1e9a
Device Details
"Udek" Ines multi-branch stent graft system
TW: โๅชๅพทๅ
โ ไผๆฉๆฏๅคๅๆฏ่ฆ่ๆฏๆถ็ณป็ตฑ
Risk Class 3

