"Baonan" non-polar interridge decompression system type I - Taiwan Registration 9ee05f6588d9b38bf6f6b96e840fcab0

Access comprehensive regulatory information for "Baonan" non-polar interridge decompression system type I in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ee05f6588d9b38bf6f6b96e840fcab0 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH 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.