"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..
This page provides complete technical specifications, regulatory compliance details. 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.
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f54555150f0cfbd42e9d951a15cf084f
Registration Details
Taiwan FDA Registration: f54555150f0cfbd42e9d951a15cf084f
Device Details
"Le See" corneal electrode
TW: โๆจๅฏ่ฆโ ่ง่้ปๆฅต
Risk Class 2

