Taiwan FDA registration 9e6a5f2205ce7a9bbeb14260dd138a45
"Nidek" corneal mapper (unsterilized)
TW: “尼德克” 角膜地圖儀 (未滅菌)
Taiwan·Risk Class 1·NIDEK TECHNOLOGIES S.R.L.·Registered Apr 23, 2010 – Apr 23, 2025CancelledRegistration details
- Analysis ID
- 9e6a5f2205ce7a9bbeb14260dd138a45
- Customs Code
- DHA04400876702
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 Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Apr 23, 2010
- Expiry Date
- Apr 23, 2025
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Nidek" corneal mapper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9e6a5f2205ce7a9bbeb14260dd138a45 and manufactured by NIDEK TECHNOLOGIES S.R.L.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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