"Fasio" intraocular lens guide (sterilization) - Taiwan Registration a23075a6eea360e4a9e66272f103e469
Access comprehensive regulatory information for "Fasio" intraocular lens 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 a23075a6eea360e4a9e66272f103e469 and manufactured by PHYSIOL S.A.. The authorized representative in Taiwan is CHIU HO SCIENTIFIC 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.
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
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Nov 25, 2016
Nov 25, 2026

