Taiwan FDA registration e30460e94cd241f7f7005e93889c0c3a
Eyelash preloaded intraocular lens implantation system
TW: 愛視睫預載式人工水晶體植入系統
Taiwan·Risk Class 3·ICARES MEDICUS, INC.·Registered Dec 12, 2017 – Dec 12, 2027ActiveRegistration details
- Analysis ID
- e30460e94cd241f7f7005e93889c0c3a
Company information
- Manufacturer
- ICARES MEDICUS, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ICARES MEDICUS, INC.
Product details
- Intended Use
- Details such as changes in the efficacy, use or indication of the approved Chinese copy sheet: Details such as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on December 7, 111 will be withdrawn and invalidated).
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- Domestic;; Security surveillance
Dates and status
- Registration Date
- Dec 12, 2017
- Expiry Date
- Dec 12, 2027
About this record
Access comprehensive regulatory information for Eyelash preloaded intraocular lens implantation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e30460e94cd241f7f7005e93889c0c3a and manufactured by ICARES MEDICUS, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..
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