"Bausch & Len" Ansie can be artificial vitreous - Taiwan Registration 757eb6ac5b3ac387378171723ca867ea

Access comprehensive regulatory information for "Bausch & Len" Ansie can be artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 757eb6ac5b3ac387378171723ca867ea and manufactured by LIFECORE BIOMEDICAL, INC.;; BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MANUFACTURED BY ANIKA THERAPEUTICS, INC. FOR BAUSCH & LOMB INC., and 1 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.