Taiwan FDA registration cb64a5bee4dc631c541e3ec0c5a8c177
“Nidek”Corneal Topography (Non-Sterile)
TW: “尼德克” 角膜地圖儀 (未滅菌)
Taiwan·Risk Class 1·MD·NIDEK TECHNOLOGIES S.R.L.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- cb64a5bee4dc631c541e3ec0c5a8c177
- License Form
- Ministry of Health Medical Device Import Registration No. 008767
- Customs Code
- DHA08400876702
Company information
- Manufacturer
- NIDEK TECHNOLOGIES S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- IKI MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
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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