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"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.

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3c3726f3fabcb1e9d9b5cd580f2de3e8
Registration Details
Taiwan FDA Registration: 3c3726f3fabcb1e9d9b5cd580f2de3e8
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Device Details

"Optikon" Keratoscope (Non-Sterile)
TW: "ๅฅงๅบท" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3c3726f3fabcb1e9d9b5cd580f2de3e8

Ministry of Health Medical Device Import Registration No. 009323

DHA08400932307

Company Information

Italy

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