“Aesculap” Urethral dilator accessories (Non-sterile) - Taiwan Registration df690350515738a4b70af93d788538e0

Access comprehensive regulatory information for “Aesculap” Urethral dilator accessories (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number df690350515738a4b70af93d788538e0 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN 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.