"Ne-Yo" annular skull fixator - Taiwan Registration f740e3bd2f78e6ab05265b4eb7e589f3

Access comprehensive regulatory information for "Ne-Yo" annular skull fixator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f740e3bd2f78e6ab05265b4eb7e589f3 and manufactured by Neos Surgery S.L.. The authorized representative in Taiwan is BUTICON INTERNATIONAL 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.