Taiwan FDA registration d27218c3f4ff2a6c038c70512c8a98ce
“Hanita”Intensity Intraocular Lens
TW: “漢寧達”易視能人工水晶體
Taiwan·Risk Class 3·MD·Hanita Lenses·Registered Nov 21, 2022 – Nov 21, 2027ActiveRegistration details
- Analysis ID
- d27218c3f4ff2a6c038c70512c8a98ce
- License Form
- Ministry of Health Medical Device Import No. 036052
- Customs Code
- DHA05603605207
Company information
- Manufacturer
- Hanita Lenses
- Manufacturer Country
- Israel
- Authorized Representative
- OCU-MED INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 21, 2022
- Expiry Date
- Nov 21, 2027
About this record
Access comprehensive regulatory information for “Hanita”Intensity 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 d27218c3f4ff2a6c038c70512c8a98ce and manufactured by Hanita Lenses. The authorized representative in Taiwan is OCU-MED INC..
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