"Ruita" intraocular lens guide (sterilization) - Taiwan Registration fc61334475bbcb96866d8e6893f73ddc
Access comprehensive regulatory information for "Ruita" 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 fc61334475bbcb96866d8e6893f73ddc and manufactured by RET, INC.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including R.E.T., 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.
Device Details
Registration Details
fc61334475bbcb96866d8e6893f73ddc
DHA09402285105
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
Jul 18, 2022
Jul 18, 2027