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“B. Braun” Aesculap CeSPACE XP Anterior Cervical Interbody Fusion System - Taiwan Registration ed7784c0bd3f1e18ff90752155659bae

Access comprehensive regulatory information for “B. Braun” Aesculap CeSPACE XP Anterior Cervical 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 ed7784c0bd3f1e18ff90752155659bae and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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ed7784c0bd3f1e18ff90752155659bae
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Taiwan FDA Registration: ed7784c0bd3f1e18ff90752155659bae
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Device Details

“B. Braun” Aesculap CeSPACE XP Anterior Cervical Interbody Fusion System
TW: “柏朗”雅氏頸椎前路椎間融合系統
Risk Class 2
MD

Registration Details

ed7784c0bd3f1e18ff90752155659bae

Ministry of Health Medical Device Import No. 030113

DHA05603011300

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

Aug 16, 2017

Aug 16, 2027