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“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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e72087eb69e6629dab29f97478836f63
Registration Details
Taiwan FDA Registration: e72087eb69e6629dab29f97478836f63
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Device Details

“B. Braun” Aesculap PROSPACE XP Posterior Interbody Fusion System
TW: “柏朗”雅氏後路椎間盤融合系統
Risk Class 2
MD

Registration Details

e72087eb69e6629dab29f97478836f63

Ministry of Health Medical Device Import No. 032544

DHA05603254408

Company Information

Germany

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