“Waldmann” Ultraviolet-therapy Apparatus - Taiwan Registration fda0137e1e1e423904deca6c68fe3d34

Access comprehensive regulatory information for “Waldmann” Ultraviolet-therapy Apparatus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fda0137e1e1e423904deca6c68fe3d34 and manufactured by HERBERT WALDMANN GMBH& CO. KG. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HERBERT WALDMANN GMBH& CO. KG, and 2 recent registrations in the same category. 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.