Anker called out - Taiwan Registration 3b94f4dd713ae590f6c4b07bcd095a32

Access comprehensive regulatory information for Anker called out in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b94f4dd713ae590f6c4b07bcd095a32 and manufactured by AMCAD BIOMED CORPORATION. The authorized representative in Taiwan is AMCAD BIOMED 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.