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"Le See" corneal electrode - Taiwan Registration f54555150f0cfbd42e9d951a15cf084f

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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f54555150f0cfbd42e9d951a15cf084f
Registration Details
Taiwan FDA Registration: f54555150f0cfbd42e9d951a15cf084f
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Device Details

"Le See" corneal electrode
TW: โ€œๆจ‚ๅฏ่ฆ–โ€ ่ง’่†œ้›ปๆฅต
Risk Class 2

Registration Details

f54555150f0cfbd42e9d951a15cf084f

DHA05603478106

Company Information

United States;;Switzerland

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.1220 Corneal electrode

Input;; Contract manufacturing

Dates and Status

Aug 06, 2021

Aug 06, 2026