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“Optikon” Combined Eye Surgery System - Taiwan Registration 04fff018bd68ddb79841b3547d121422

Access comprehensive regulatory information for “Optikon” Combined Eye Surgery System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 04fff018bd68ddb79841b3547d121422 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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04fff018bd68ddb79841b3547d121422
Registration Details
Taiwan FDA Registration: 04fff018bd68ddb79841b3547d121422
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Device Details

“Optikon” Combined Eye Surgery System
TW: “奧康”眼科手術儀
Risk Class 2
MD

Registration Details

04fff018bd68ddb79841b3547d121422

Ministry of Health Medical Device Import No. 029266

DHA05602926609

Company Information

Italy

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M4670 Crystal Emulsifier

Imported from abroad

Dates and Status

Jan 05, 2017

Jan 05, 2027