Taiwan FDA registration 9e50c71e53ca64c7306a31bf66b0cc6e
“OPTIKON” Keratron Corneal Topographer (Non-sterile)
TW: “奧帝康”科瑞創角膜地圖儀 (未滅菌)
Taiwan·Risk Class 1·MD·OPTIKON 2000 S. P. A.·Registered Jan 28, 2014 – Jan 28, 2019CancelledRegistration details
- Analysis ID
- 9e50c71e53ca64c7306a31bf66b0cc6e
- License Form
- Ministry of Health Medical Device Import No. 013820
- Customs Code
- DHA09401382006
Company information
- Manufacturer
- OPTIKON 2000 S. P. A.
- Manufacturer Country
- Italy
- Authorized Representative
- WINSTON MEDICAL SUPPLY CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 28, 2014
- Expiry Date
- Jan 28, 2019
- Cancellation Date
- Jan 14, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
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 9e50c71e53ca64c7306a31bf66b0cc6e and manufactured by OPTIKON 2000 S. P. A.. The authorized representative in Taiwan is WINSTON MEDICAL SUPPLY CO., LTD..
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