"Serucon" coronary angioplasty balloon catheter - Taiwan Registration b0e520aafbdad80369953bd730bb35bd
Access comprehensive regulatory information for "Serucon" coronary angioplasty 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 b0e520aafbdad80369953bd730bb35bd and manufactured by MedAlliance LLC;; MedAlliance CardioVascular SA. The authorized representative in Taiwan is REGISTAR CO., LTD..
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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b0e520aafbdad80369953bd730bb35bd
Registration Details
Taiwan FDA Registration: b0e520aafbdad80369953bd730bb35bd
Device Details
"Serucon" coronary angioplasty balloon catheter
TW: โ็็ๆฝฏโๅ ็ๅ่ๆๅฝข่ก็ๅๅฐ็ฎก
Risk Class 2

