Taiwan FDA registration 0ce90abe92b0d14ca58800b989dbe429
Eyelash multifocal astigmatism corrected intraocular lens
TW: 愛視睫多焦點散光矯正型人工水晶體
Taiwan·Risk Class 3·ICARES MEDICUS, INC.·Registered Mar 28, 2022 – Mar 28, 2027CancelledRegistration details
- Analysis ID
- 0ce90abe92b0d14ca58800b989dbe429
Company information
- Manufacturer
- ICARES MEDICUS, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ICARES MEDICUS, INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- Domestic;; Security surveillance
Dates and status
- Registration Date
- Mar 28, 2022
- Expiry Date
- Mar 28, 2027
- Cancellation Date
- Oct 29, 2024
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Eyelash multifocal 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 0ce90abe92b0d14ca58800b989dbe429 and manufactured by ICARES MEDICUS, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..
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