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“Syrison” Interbody Fusion System - Taiwan Registration b40e2259c8cf8231cba8f706aa3f4f70

Access comprehensive regulatory information for “Syrison” 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 b40e2259c8cf8231cba8f706aa3f4f70 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM CO., LTD..

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b40e2259c8cf8231cba8f706aa3f4f70
Registration Details
Taiwan FDA Registration: b40e2259c8cf8231cba8f706aa3f4f70
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Device Details

“Syrison” Interbody Fusion System
TW: “喜瑞森”椎間融合系統
Risk Class 2
MD

Registration Details

b40e2259c8cf8231cba8f706aa3f4f70

Ministry of Health Medical Device Manufacturing No. 006536

Company Information

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Produced in Taiwan, China

Dates and Status

Oct 30, 2019

Oct 30, 2024