“Penumbra” Penumbra System - Taiwan Registration d2ab06a194322a826a5b56338350f154

Access comprehensive regulatory information for “Penumbra” Penumbra System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2ab06a194322a826a5b56338350f154 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.