Taiwan FDA registration cc4870c2fd03e9e25907b3aced7b7421
"Haninda" intraocular lens guide (sterilization)
TW: "漢寧達" 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·HANITA LENSES·Registered Apr 28, 2015 – Apr 28, 2025ExpiredRegistration details
- Analysis ID
- cc4870c2fd03e9e25907b3aced7b7421
- Customs Code
- DHA09401516803
Company information
- Manufacturer
- HANITA LENSES
- Manufacturer Country
- Israel
- Authorized Representative
- OCU-MED INC.
Product details
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 28, 2015
- Expiry Date
- Apr 28, 2025
About this record
Access comprehensive regulatory information for "Haninda" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cc4870c2fd03e9e25907b3aced7b7421 and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED INC..
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