"Biose" titanium dioxide hernia repair net - Taiwan Registration e89354737c7a540c48e766da04c394db

Access comprehensive regulatory information for "Biose" titanium dioxide hernia repair net in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e89354737c7a540c48e766da04c394db and manufactured by BIOCER ENTWICKLUNGS-GMBH. The authorized representative in Taiwan is HEALTH RIVER 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.