Taiwan FDA registration 21ec8a4741fc3508fd63cbe20e6ecac8
"Ostic" Atichen intraocular lens
TW: “歐斯提克”阿提申人工水晶體
Taiwan·Risk Class 3·OPHTEC B.V.·Registered Aug 14, 2007 – Aug 14, 2027ActiveRegistration details
- Analysis ID
- 21ec8a4741fc3508fd63cbe20e6ecac8
- Customs Code
- DHA00601841407
Company information
- Manufacturer
- OPHTEC B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- It is suitable for patients with stable correction of myopia and myopic astigmatism and who cannot achieve a satisfactory level with glasses or contact lenses.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Aug 14, 2007
- Expiry Date
- Aug 14, 2027
About this record
Access comprehensive regulatory information for "Ostic" Atichen 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 21ec8a4741fc3508fd63cbe20e6ecac8 and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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