“B. Braun” Aesculap PROSPACE XP Posterior Interbody Fusion System - Taiwan Registration e72087eb69e6629dab29f97478836f63
Access comprehensive regulatory information for “B. Braun” Aesculap PROSPACE XP Posterior 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 e72087eb69e6629dab29f97478836f63 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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Device Details
Registration Details
e72087eb69e6629dab29f97478836f63
Ministry of Health Medical Device Import No. 032544
DHA05603254408
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedic devices
N3080 Interbody fusion device
Imported from abroad
Dates and Status
May 12, 2019
May 12, 2024

