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“Wiltrom” Vertebral Body Augmentation System - Taiwan Registration ed3901c73e0d1b5d46914d14ef4602f2

Access comprehensive regulatory information for “Wiltrom” Vertebral Body Augmentation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed3901c73e0d1b5d46914d14ef4602f2 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM CO., LTD..

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ed3901c73e0d1b5d46914d14ef4602f2
Registration Details
Taiwan FDA Registration: ed3901c73e0d1b5d46914d14ef4602f2
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Device Details

“Wiltrom” Vertebral Body Augmentation System
TW: “威創”可擴張椎體強化系統
Risk Class 2
MD

Registration Details

ed3901c73e0d1b5d46914d14ef4602f2

Ministry of Health Medical Device Manufacturing No. 006324

Company Information

Product Details

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

N Orthopedic devices

N3060 Spine correction fixation between vertebral bodies

Produced in Taiwan, China

Dates and Status

Mar 18, 2019

Dec 08, 2028