"Ruita" intraocular lens guide (sterilization) - Taiwan Registration 13c56421f65126ef180396ac929e7468
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 13c56421f65126ef180396ac929e7468 and manufactured by R.E.T., INC.. The authorized representative in Taiwan is SHENG SHIUAN INDUSTRIAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RET, 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
13c56421f65126ef180396ac929e7468
DHA09401518707
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
Input;; QMS/QSD
Dates and Status
May 01, 2015
May 01, 2030