"EyeSys" Corneal Topography System (Non-Sterile)
Taiwan·Risk Class 1·MD·EYESYS VISION, INC.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- cb8317c0c8caa99fe3bdd72f5e5c0097
- License Form
- Ministry of Health Medical Device Import Registration No. 016285
- Customs Code
- DHA08401628503
- Manufacturer
- EYESYS VISION, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EVERVISION INSTRUMENT CO.
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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.