Taiwan FDA registration 9d796486d765d8d4273028f2c947d234
"Aiken" clearly sees artificial vitreous
TW: “艾肯”明妥見人工玻璃體
Taiwan·Risk Class 3·EyeKon Medical, Inc.;; EyeKon Medical, Ltd.·Registered Jun 05, 2014 – Jun 05, 2019CancelledRegistration details
- Analysis ID
- 9d796486d765d8d4273028f2c947d234
- Customs Code
- DHA05602623101
Company information
- Manufacturer
- EyeKon Medical, Inc.;; EyeKon Medical, Ltd.
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- COSMOS BIO, 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.4275 眼內充填用液體
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Jun 05, 2014
- Expiry Date
- Jun 05, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aiken" clearly sees artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9d796486d765d8d4273028f2c947d234 and manufactured by EyeKon Medical, Inc.;; EyeKon Medical, Ltd.. The authorized representative in Taiwan is COSMOS BIO, INC..
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