“Sebia” IT/IF Control - Taiwan Registration 744c30cbc093ebf7cbb53123a7f483a8

Access comprehensive regulatory information for “Sebia” IT/IF Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 744c30cbc093ebf7cbb53123a7f483a8 and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech 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.