“Aesculap” 3D Interbody Fusion System - Taiwan Registration 05bd4dc4d83a3a2cdf85889182a46606

Access comprehensive regulatory information for “Aesculap” 3D Interbody Fusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05bd4dc4d83a3a2cdf85889182a46606 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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