"EyeSys" Corneal Topography (Non-Sterile)
Taiwan·Risk Class 1·MD·EYESYS VISION, INC.·Registered Apr 18, 2018 – Apr 18, 2023Cancelled- Analysis ID
- 84c43b8ce967c0a7431caae9e7b5bab8
- License Form
- Ministry of Health Medical Device Import No. 018982
- Customs Code
- DHA09401898205
- Manufacturer
- EYESYS VISION, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Apr 18, 2018
- Expiry Date
- Apr 18, 2023
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 84c43b8ce967c0a7431caae9e7b5bab8 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.