"Bausch & Len" IOL Guide (Sterilization) - Taiwan Registration 47857bb98c0a6d0e8ec09f1ee1eaccc4
Access comprehensive regulatory information for "Bausch & Len" IOL Guide (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 47857bb98c0a6d0e8ec09f1ee1eaccc4 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BAUSCH & LOMB INC., MEDICEL AT, 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.
Device Details
Product Details
Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
M Ophthalmology
M.4300 Artificial crystal body inducer
import
Dates and Status
Apr 13, 2006
Apr 13, 2026