Taiwan FDA registration c41960f84af1c611fa705024b8ee44dc
"Fidia" Al vitreous replacement
TW: "菲迪雅" 艾爾玻璃體替代物
Taiwan·FIDIA FARMACEUTICI S.P.A.·Registered Jan 18, 2002 – Jan 18, 2007CancelledRegistration details
- Analysis ID
- c41960f84af1c611fa705024b8ee44dc
- Customs Code
- DHA00600980903
Company information
- Manufacturer
- FIDIA FARMACEUTICI S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MED PHARMA CO., LTD.
Product details
- Intended Use
- Suitable for use in anterior or posterior chamber surgery and removed before surgery is completed.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2002
- Expiry Date
- Jan 18, 2007
- Cancellation Date
- Nov 09, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fidia" Al vitreous replacement in Taiwan's medical device market through Pure Global AI's free database. is registered under number c41960f84af1c611fa705024b8ee44dc and manufactured by FIDIA FARMACEUTICI S.P.A.. The authorized representative in Taiwan is MED PHARMA CO., LTD..
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