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“BAAT” Fortilink-SA with TiPlus Technolgy Anterior Lumbar Cage - Taiwan Registration 41ad3eea9548408ea0ea6dc06eae560f

Access comprehensive regulatory information for “BAAT” Fortilink-SA with TiPlus Technolgy Anterior Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41ad3eea9548408ea0ea6dc06eae560f and manufactured by Baat Medical Products B.V.. The authorized representative in Taiwan is PARADIGM SPINE TAIWAN 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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41ad3eea9548408ea0ea6dc06eae560f
Registration Details
Taiwan FDA Registration: 41ad3eea9548408ea0ea6dc06eae560f
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Device Details

“BAAT” Fortilink-SA with TiPlus Technolgy Anterior Lumbar Cage
TW: “百適”弗帝希腰椎系統前路腰椎融合裝置
Risk Class 2
MD

Registration Details

41ad3eea9548408ea0ea6dc06eae560f

Ministry of Health Medical Device Import No. 036288

DHA05603628800

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3060 Spine correction fixation between vertebral bodies

Imported from abroad

Dates and Status

Jan 18, 2023

Jan 18, 2028