"Medtronic" Kaifeng expansion syringe - Taiwan Registration 2725c19cf35303fd1ffe0235b88841c7

Access comprehensive regulatory information for "Medtronic" Kaifeng expansion syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2725c19cf35303fd1ffe0235b88841c7 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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.