Taiwan FDA registration 6b7056744e61da16beaca6d3e4f4a19e
“Hanita” SeeLens AF Aspheric Hydrophilic Intraocular Lens
TW: “漢寧達”愛視能非球面人工水晶體
Taiwan·Risk Class 3·MD·HANITA LENSES·Registered Apr 01, 2015 – Apr 01, 2025ExpiredRegistration details
- Analysis ID
- 6b7056744e61da16beaca6d3e4f4a19e
- License Form
- Ministry of Health Medical Device Import No. 027248
- Customs Code
- DHA05602724800
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 01, 2015
- Expiry Date
- Apr 01, 2025
About this record
Access comprehensive regulatory information for “Hanita” SeeLens AF 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 6b7056744e61da16beaca6d3e4f4a19e and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices