Taiwan FDA registration ed6fac462997968d4aa3b6b2d8585bef
"Oticon" Kerutron corneal mapper (unsterilized)
TW: “奧蒂康”科瑞創角膜地圖儀（未滅菌）
Taiwan·Risk Class 1·OPTIKON 2000 S. P. A·Registered Mar 21, 2011 – Mar 21, 2026CancelledRegistration details
- Analysis ID
- ed6fac462997968d4aa3b6b2d8585bef
- Customs Code
- DHA04401005702
Company information
- Manufacturer
- OPTIKON 2000 S. P. A
- Manufacturer Country
- Italy
- Authorized Representative
- OPTACT INTERNATIONAL 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
- Mar 21, 2011
- Expiry Date
- Mar 21, 2026
- 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 "Oticon" Kerutron 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 ed6fac462997968d4aa3b6b2d8585bef and manufactured by OPTIKON 2000 S. P. A. The authorized representative in Taiwan is OPTACT INTERNATIONAL CO., LTD..
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