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“Nidek”Corneal Topography (Non-Sterile) - Taiwan Registration cb64a5bee4dc631c541e3ec0c5a8c177

Access comprehensive regulatory information for “Nidek”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 cb64a5bee4dc631c541e3ec0c5a8c177 and manufactured by NIDEK TECHNOLOGIES S.R.L.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

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cb64a5bee4dc631c541e3ec0c5a8c177
Registration Details
Taiwan FDA Registration: cb64a5bee4dc631c541e3ec0c5a8c177
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Device Details

“Nidek”Corneal Topography (Non-Sterile)
TW: “尼德克” 角膜地圖儀 (未滅菌)
Risk Class 1
MD

Registration Details

cb64a5bee4dc631c541e3ec0c5a8c177

Ministry of Health Medical Device Import Registration No. 008767

DHA08400876702

Company Information

Italy

Product Details

Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025