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“BAAT” Fortilink-L with TiPlus Technology Lateral Lumbar Cage - Taiwan Registration 35d16ff8d09e9bf48580f47a0f023ba2

Access comprehensive regulatory information for “BAAT” Fortilink-L with TiPlus Technology Lateral 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 35d16ff8d09e9bf48580f47a0f023ba2 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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35d16ff8d09e9bf48580f47a0f023ba2
Registration Details
Taiwan FDA Registration: 35d16ff8d09e9bf48580f47a0f023ba2
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Device Details

“BAAT” Fortilink-L with TiPlus Technology Lateral Lumbar Cage
TW: “百適”弗帝希腰椎系統側位融合裝置
Risk Class 2
MD

Registration Details

35d16ff8d09e9bf48580f47a0f023ba2

Ministry of Health Medical Device Import No. 036141

DHA05603614106

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

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Imported from abroad

Dates and Status

Dec 21, 2022

Dec 21, 2027