JBone Interbody Fusion Device System - Taiwan Registration a69616d899f68007ef1e8f0e10de79f9

Access comprehensive regulatory information for JBone Interbody Fusion Device System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a69616d899f68007ef1e8f0e10de79f9 and manufactured by JBone Biotechnology Co.,Ltd.. The authorized representative in Taiwan is JBone Biotechnology 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.