"Guanya" hollow intervertebral fusion device - Taiwan Registration 2fa89889426fce733d7e45783bafcd7c

Access comprehensive regulatory information for "Guanya" hollow intervertebral fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2fa89889426fce733d7e45783bafcd7c and manufactured by A-SPINE Asia Co., Ltd.. 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.