“Kaneka” i-ED COIL System - Taiwan Registration a6f080241c73b84c1501f2941f45a837

Access comprehensive regulatory information for “Kaneka” i-ED COIL System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a6f080241c73b84c1501f2941f45a837 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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.