Reinter IOL guide (sterilization) - Taiwan Registration 5fedb129b93056aad5be821305aad2be
Access comprehensive regulatory information for Reinter 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 5fedb129b93056aad5be821305aad2be and manufactured by RET, INC.. The authorized representative in Taiwan is CRYSTALVISION CO., LTD..
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Device Details
Registration Details
5fedb129b93056aad5be821305aad2be
DHA09402295902
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 17, 2022
Nov 17, 2027