"Fidia" knee interarticular injection - Taiwan Registration 4043e7d4cde7e6a78b086756c8c82608
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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Device Details
Product Details
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.
N Orthopedics
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Dates and Status
Feb 03, 2004
Feb 03, 2029