Taiwan FDA registration 4043e7d4cde7e6a78b086756c8c82608
"Fidia" knee interarticular injection
TW: "菲迪雅" 膝爾康關節腔注射劑
Taiwan·Risk Class 3·FIDIA FARMACEUTICI ITALIANI S.P.A.·Registered Feb 03, 2004 – Feb 03, 2029ActiveRegistration details
- Analysis ID
- 4043e7d4cde7e6a78b086756c8c82608
- Customs Code
- DHA00601053008
Company information
- Manufacturer
- FIDIA FARMACEUTICI ITALIANI S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MED PHARMA CO., LTD.
Product details
- Intended Use
- Treatment of patients with degenerative knee arthritis pain is limited to conservative non-pharmacological treatments and general analgesics such as ACETAMINOPHEN that do not respond to the response.
- Product Type (Level 1)
- N Orthopedics
- Unit
- 預充式注射針筒;;小瓶
- Import Information
- import
Dates and status
- Registration Date
- Feb 03, 2004
- Expiry Date
- Feb 03, 2029
About this record
Access comprehensive regulatory information for "Fidia" knee interarticular injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4043e7d4cde7e6a78b086756c8c82608 and manufactured by FIDIA FARMACEUTICI ITALIANI S.P.A.. The authorized representative in Taiwan is MED PHARMA CO., LTD..
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