Taiwan FDA registration 38a39de0c221af0071853d2dbe6ace2a
Eyelash trifocal intraocular lens
TW: 愛視睫三焦點人工水晶體
Registration details
- Analysis ID
- 38a39de0c221af0071853d2dbe6ace2a
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
- Apr 23, 2021
- Expiry Date
- Apr 23, 2026
About this record
Access comprehensive regulatory information for Eyelash trifocal 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 38a39de0c221af0071853d2dbe6ace2a and manufactured by ICARES MEDICUS, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..
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