“Penumbra” Ruby Coil System - Taiwan Registration 1a20a601e1b547967728c8047b56f9e9

Access comprehensive regulatory information for “Penumbra” Ruby Coil System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1a20a601e1b547967728c8047b56f9e9 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.