"RET" Intraocular Lens Guide (Non-Sterile) - Taiwan Registration 93137ca76767043ed0547fcec6edab60
Access comprehensive regulatory information for "RET" Intraocular Lens Guide (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 93137ca76767043ed0547fcec6edab60 and manufactured by RET, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..
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
93137ca76767043ed0547fcec6edab60
Ministry of Health Medical Device Import No. 017755
DHA09401775502
Product Details
Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
M Ophthalmic devices
M4300 Intraocular Lens Guide
Imported from abroad
Dates and Status
Apr 24, 2017
Apr 24, 2022

