Taiwan FDA registration f54555150f0cfbd42e9d951a15cf084f
"Le See" corneal electrode
TW: “樂可視” 角膜電極
Taiwan·Risk Class 2·Fabrinal SA;; LKC TECHNOLOGIES, INC.·Registered Aug 06, 2021 – Aug 06, 2026ActiveRegistration details
- Analysis ID
- f54555150f0cfbd42e9d951a15cf084f
- Customs Code
- DHA05603478106
Company information
- Manufacturer
- Fabrinal SA;; LKC TECHNOLOGIES, INC.
- Manufacturer Country
- United States;;Switzerland
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1220 Corneal electrode
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Aug 06, 2021
- Expiry Date
- Aug 06, 2026
About this record
Access comprehensive regulatory information for "Le See" corneal electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f54555150f0cfbd42e9d951a15cf084f and manufactured by Fabrinal SA;; LKC TECHNOLOGIES, INC.. The authorized representative in Taiwan is CLINICO INC..
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