Taiwan FDA registration fa9274173f58b5431fb79f68e6c71344
“Hanita” SeeLens MF Aspheric Multifocal Intraocular Lens
TW: “漢寧達”全視能非球面多焦點人工水晶體
Taiwan·Risk Class 3·MD·HANITA LENSES·Registered Apr 02, 2015 – Apr 02, 2025ExpiredRegistration details
- Analysis ID
- fa9274173f58b5431fb79f68e6c71344
- License Form
- Ministry of Health Medical Device Import No. 027251
- Customs Code
- DHA05602725102
Company information
- Manufacturer
- HANITA LENSES
- Manufacturer Country
- Israel
- Authorized Representative
- OCU-MED INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 02, 2015
- Expiry Date
- Apr 02, 2025
About this record
Access comprehensive regulatory information for “Hanita” SeeLens MF Aspheric Multifocal 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 fa9274173f58b5431fb79f68e6c71344 and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED INC..
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