“Penumbra” 3D Revascularization Device - Taiwan Registration b0aef1b0f2832ab85c52e80ae94d5746

Access comprehensive regulatory information for “Penumbra” 3D Revascularization Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0aef1b0f2832ab85c52e80ae94d5746 and manufactured by PENUMBRA, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..

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.