"Gusha" Pareki substrate - Taiwan Registration 3f3e7be934531e01dd6cedbc15860d7e

Access comprehensive regulatory information for "Gusha" Pareki substrate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f3e7be934531e01dd6cedbc15860d7e and manufactured by Kulzer GmbH;; Kulzer SRL. The authorized representative in Taiwan is TEI JEL ENTERPRISE CO., LTD..

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.