Taiwan FDA registration 2964924c85e98aeec27d74cc508a0e59
"Optic" ophthalmic laser system
TW: “歐普特”眼科雷射系統
Taiwan·Risk Class 2·OPTOTEK D.O.O.·Registered Aug 29, 2011 – Aug 29, 2026ActiveRegistration details
- Analysis ID
- 2964924c85e98aeec27d74cc508a0e59
- Customs Code
- DHA00602276703
Company information
- Manufacturer
- OPTOTEK D.O.O.
- Manufacturer Country
- Slovenia
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4390 眼科雷射裝置
- Import Information
- import
Dates and status
- Registration Date
- Aug 29, 2011
- Expiry Date
- Aug 29, 2026
About this record
Access comprehensive regulatory information for "Optic" ophthalmic laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2964924c85e98aeec27d74cc508a0e59 and manufactured by OPTOTEK D.O.O.. The authorized representative in Taiwan is CLINICO INC..
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