"Optikon" Keratoscope (Non-Sterile) - Taiwan Registration 3c3726f3fabcb1e9d9b5cd580f2de3e8
Access comprehensive regulatory information for "Optikon" Keratoscope (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 3c3726f3fabcb1e9d9b5cd580f2de3e8 and manufactured by OPTIKON 2000 S. P. A. The authorized representative in Taiwan is CLINICO INC..
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
Registration Details
3c3726f3fabcb1e9d9b5cd580f2de3e8
Ministry of Health Medical Device Import Registration No. 009323
DHA08400932307
Product Details
Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
M Ophthalmic devices
M1350 Keatoscope
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2025

