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“Wiltrom” Cerapeek Interbody Fusion System - Taiwan Registration 7867aae16d0eb08bb654b5bdd3ac984e

Access comprehensive regulatory information for “Wiltrom” Cerapeek 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 7867aae16d0eb08bb654b5bdd3ac984e and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM CO., LTD..

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7867aae16d0eb08bb654b5bdd3ac984e
Registration Details
Taiwan FDA Registration: 7867aae16d0eb08bb654b5bdd3ac984e
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Device Details

“Wiltrom” Cerapeek Interbody Fusion System
TW: “台微醫”有陶式椎間融合系統
Risk Class 2
MD

Registration Details

7867aae16d0eb08bb654b5bdd3ac984e

Ministry of Health Medical Device Manufacturing No. 006512

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

Jun 17, 2019

Jun 17, 2024