Taiwan FDA registration 1b14de22e2044b4b77ce0611062f729f
"Ostic" Atifix intraocular lens
TW: “歐斯提克”阿提菲克斯人工水晶體
Registration details
- Analysis ID
- 1b14de22e2044b4b77ce0611062f729f
- Customs Code
- DHA00602112102
Company information
- Manufacturer
- OPHTEC B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
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.3600 Artificial Crystal
- Import Information
- import
Dates and status
- Registration Date
- Jun 11, 2010
- Expiry Date
- Jun 11, 2025
About this record
Access comprehensive regulatory information for "Ostic" Atifix intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1b14de22e2044b4b77ce0611062f729f and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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