Taiwan FDA registration eb31a97bfd2b7956d6b59ba3f8dad264
"Hanent" folded intraocular lens
TW: “翰能特”折疊式人工水晶體
Taiwan·Risk Class 3·HANITA LENSES·Registered Mar 30, 2007 – Mar 30, 2012CancelledRegistration details
- Analysis ID
- eb31a97bfd2b7956d6b59ba3f8dad264
- Customs Code
- DHA00601797401
Company information
- Manufacturer
- HANITA LENSES
- Manufacturer Country
- Israel
- Authorized Representative
- CHI FU TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- import
Dates and status
- Registration Date
- Mar 30, 2007
- Expiry Date
- Mar 30, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hanent" folded 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 eb31a97bfd2b7956d6b59ba3f8dad264 and manufactured by HANITA LENSES. The authorized representative in Taiwan is CHI FU TRADING CO., LTD..
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