"Xinli" guide wire - Taiwan Registration b0fa85e84b6f16384d6bf4eea57d380f

Access comprehensive regulatory information for "Xinli" guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0fa85e84b6f16384d6bf4eea57d380f and manufactured by Sunny Medical Device (Shenzhen) Co., Ltd.. The authorized representative in Taiwan is CATHERINE CONSULTANTS 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.