"EyeSys" Corneal Topography (Non-Sterile)
Taiwan·Risk Class 1·MD·EYESYS VISION, INC.·Registered Jul 22, 2014 – Jul 22, 2019Cancelled- Analysis ID
- 249b759ad0a530f76b21283e2141c602
- License Form
- Ministry of Health Medical Device Import No. 014352
- Customs Code
- DHA09401435204
- Manufacturer
- EYESYS VISION, INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAY HUNG INSTRUMENT CO., LTD.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Jul 22, 2014
- Expiry Date
- Jul 22, 2019
- Cancellation Date
- Jun 22, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 249b759ad0a530f76b21283e2141c602 and manufactured by EYESYS VISION, INC.. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..
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.