Taiwan FDA registration 973ac7e87f0ce511e7798b7886ef8032
"Aikneekang" disposable autologous cartilage repair system
TW: “愛膝康”一次性自體軟骨修補系統
Taiwan·Risk Class 3·BIOGEND THERAPEUTICS CO., LTD.·Registered Apr 23, 2020 – Apr 23, 2030ActiveRegistration details
- Analysis ID
- 973ac7e87f0ce511e7798b7886ef8032
Company information
- Manufacturer
- BIOGEND THERAPEUTICS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOGEND THERAPEUTICS CO., LTD.
Product details
- Intended Use
- This product is suitable for filling cartilage and cartilage defects in the medial femoral condyle, lateral femoral condyle and femoral trochlear of the knee joint and helping to repair the cartilage and hard bone tissue.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.9999 Miscellaneous
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 23, 2020
- Expiry Date
- Apr 23, 2030
About this record
Access comprehensive regulatory information for "Aikneekang" disposable autologous cartilage repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 973ac7e87f0ce511e7798b7886ef8032 and manufactured by BIOGEND THERAPEUTICS CO., LTD.. The authorized representative in Taiwan is BIOGEND THERAPEUTICS CO., LTD..
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