Taiwan FDA registration d04c3638cf41c8b637a7c24417315c9a
“Hanita” SeeLens AF easy Preloaded Aspheric Hydrophilic Intraocular Lens
TW: “漢寧達”愛視預載式非球面人工水晶體
Taiwan·Risk Class 3·MD·HANITA LENSES·Registered Apr 02, 2015 – Apr 02, 2020CancelledRegistration details
- Analysis ID
- d04c3638cf41c8b637a7c24417315c9a
- License Form
- Ministry of Health Medical Device Import No. 027250
- Customs Code
- DHA05602725000
Company information
- Manufacturer
- HANITA LENSES
- Manufacturer Country
- Israel
- Authorized Representative
- OCU-MED INC.
Product details
- 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, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Hanita” SeeLens AF easy Preloaded Aspheric Hydrophilic 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 d04c3638cf41c8b637a7c24417315c9a and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED INC..
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