"EyeSys" Corneal Topography (Non-Sterile)
Taiwan·Risk Class 1·MD·EYESYS VISION, INC.·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- e81e4824d7998a52999132f273d07aa6
- License Form
- Ministry of Health Medical Device Import Registration No. 018982
- Customs Code
- DHA08401898209
- Manufacturer
- EYESYS VISION, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
- 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, 2023
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Access comprehensive regulatory information for "EyeSys" Corneal Topography (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 e81e4824d7998a52999132f273d07aa6 and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is CLINICO INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including EYESYS VISION, INC., and 2 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.