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"EyeSys" Corneal Topography System (Non-Sterile) - Taiwan Registration cb8317c0c8caa99fe3bdd72f5e5c0097

Access comprehensive regulatory information for "EyeSys" Corneal Topography System (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 cb8317c0c8caa99fe3bdd72f5e5c0097 and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EYESYS VISION, 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.

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cb8317c0c8caa99fe3bdd72f5e5c0097
Registration Details
Taiwan FDA Registration: cb8317c0c8caa99fe3bdd72f5e5c0097
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Device Details

"EyeSys" Corneal Topography System (Non-Sterile)
TW: "ๆ„›่ฆ–" ่ง’่†œๅœฐๅœ–ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

cb8317c0c8caa99fe3bdd72f5e5c0097

Ministry of Health Medical Device Import Registration No. 016285

DHA08401628503

Company Information

United States

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, 2026

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