Seevert posterior cervical fixation system - Taiwan Registration 0c4eb71cf279a1086904c29c803ba31e

Access comprehensive regulatory information for Seevert posterior cervical fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c4eb71cf279a1086904c29c803ba31e and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia 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.