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"Aikneekang" disposable autologous cartilage repair system - Taiwan Registration 973ac7e87f0ce511e7798b7886ef8032

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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973ac7e87f0ce511e7798b7886ef8032
Registration Details
Taiwan FDA Registration: 973ac7e87f0ce511e7798b7886ef8032
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Device Details

"Aikneekang" disposable autologous cartilage repair system
TW: โ€œๆ„›่†ๅบทโ€ไธ€ๆฌกๆ€ง่‡ช้ซ”่ปŸ้ชจไฟฎ่ฃœ็ณป็ตฑ
Risk Class 3

Registration Details

973ac7e87f0ce511e7798b7886ef8032

Company Information

Taiwan, Province of China

Product Details

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.

N Orthopedics

N.9999 Miscellaneous

Domestic

Dates and Status

Apr 23, 2020

Apr 23, 2030