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“BAAT” Fortilink-SC with TiPlus Technology - Taiwan Registration 3763461ac2d4fedf5f13ad2bf67be1c4

Access comprehensive regulatory information for “BAAT” Fortilink-SC with TiPlus Technology in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3763461ac2d4fedf5f13ad2bf67be1c4 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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3763461ac2d4fedf5f13ad2bf67be1c4
Registration Details
Taiwan FDA Registration: 3763461ac2d4fedf5f13ad2bf67be1c4
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Device Details

“BAAT” Fortilink-SC with TiPlus Technology
TW: “百適”弗帝希頸椎系統
Risk Class 2
MD

Registration Details

3763461ac2d4fedf5f13ad2bf67be1c4

Ministry of Health Medical Device Import No. 036104

DHA05603610400

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Nov 23, 2022

Nov 23, 2027