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“B. Braun” Aesculap TSPACE XP Interbody Fusion System - Taiwan Registration d2ac3f4f3f02ee2f459db06523c134e6

Access comprehensive regulatory information for “B. Braun” Aesculap TSPACE XP 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 d2ac3f4f3f02ee2f459db06523c134e6 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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d2ac3f4f3f02ee2f459db06523c134e6
Registration Details
Taiwan FDA Registration: d2ac3f4f3f02ee2f459db06523c134e6
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Device Details

“B. Braun” Aesculap TSPACE XP Interbody Fusion System
TW: “柏朗”雅氏椎間盤融合系統
Risk Class 2
MD

Registration Details

d2ac3f4f3f02ee2f459db06523c134e6

Ministry of Health Medical Device Import No. 031055

DHA05603105501

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3060 Spine correction fixation between vertebral bodies

Imported from abroad

Dates and Status

Apr 25, 2018

Apr 25, 2028