“Penumbra” INDIGO Aspiration System - Taiwan Registration 71e91845f2d5f0ce5a49ebf3fc00ce8e

Access comprehensive regulatory information for “Penumbra” INDIGO Aspiration System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71e91845f2d5f0ce5a49ebf3fc00ce8e and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Penumbra, Inc., and 1 recent registrations in the same category. 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.