“SDI” Aura Easyflow Ultra Universal Restorative Material - Taiwan Registration 7a1e7c0ac47b5f8a51ce9b2b845e0d7d

Access comprehensive regulatory information for “SDI” Aura Easyflow Ultra Universal Restorative Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7a1e7c0ac47b5f8a51ce9b2b845e0d7d and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH 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.