Taiwan FDA registration afe6f9d47e89b9f6a141324b37acb37f
“OPTIKON”Keratron Corneal Topographer(Non-Sterile)
TW: “奧蒂康”科瑞創角膜地圖儀（未滅菌）
Taiwan·Risk Class 1·MD·OPTIKON 2000 S. P. A·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- afe6f9d47e89b9f6a141324b37acb37f
- License Form
- Ministry of Health Medical Device Import Registration No. 010057
- Customs Code
- DHA08401005702
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 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, 2026
About this record
Access comprehensive regulatory information for “OPTIKON”Keratron Corneal Topographer(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 afe6f9d47e89b9f6a141324b37acb37f and manufactured by OPTIKON 2000 S. P. A. The authorized representative in Taiwan is OPTACT INTERNATIONAL CO., LTD..
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