Taiwan FDA registration a7e2aab9a8bf9af5e406caaa242945a9
"Ostic" Atishen amorphous intraocular lens
TW: “歐斯提克”阿提申無晶體式人工水晶體
Taiwan·Risk Class 3·OPHTEC B.V.·Registered Jun 15, 2010 – Jun 15, 2025ExpiredRegistration details
- Analysis ID
- a7e2aab9a8bf9af5e406caaa242945a9
- Customs Code
- DHA00602071003
Company information
- Manufacturer
- OPHTEC B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- Amorphous patients with insufficient posterior capsule support to place posterior chamber intraocular lenses.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Jun 15, 2010
- Expiry Date
- Jun 15, 2025
About this record
Access comprehensive regulatory information for "Ostic" Atishen amorphous 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 a7e2aab9a8bf9af5e406caaa242945a9 and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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