Taiwan FDA registration 5bef2f51374545fad92e6328ccab43cb
Eyesight eyelash astigmatism corrected intraocular lens
TW: 愛視睫散光矯正型人工水晶體
Taiwan·Risk Class 3·ICARES MEDICUS, INC.·Registered Nov 01, 2018 – Nov 01, 2028ActiveRegistration details
- Analysis ID
- 5bef2f51374545fad92e6328ccab43cb
Company information
- Manufacturer
- ICARES MEDICUS, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ICARES MEDICUS, INC.
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
- Security Surveillance;; Domestic
Dates and status
- Registration Date
- Nov 01, 2018
- Expiry Date
- Nov 01, 2028
About this record
Access comprehensive regulatory information for Eyesight eyelash astigmatism corrected 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 5bef2f51374545fad92e6328ccab43cb and manufactured by ICARES MEDICUS, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..
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