Pure Global

“BAAT” Fortilink-TS with TiPlus Technology Transforaminal/Posterior Lumbar Cage - Taiwan Registration 299bdd528d7b9b1363b46c143b728495

Access comprehensive regulatory information for “BAAT” Fortilink-TS with TiPlus Technology Transforaminal/Posterior 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 299bdd528d7b9b1363b46c143b728495 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
299bdd528d7b9b1363b46c143b728495
Registration Details
Taiwan FDA Registration: 299bdd528d7b9b1363b46c143b728495
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“BAAT” Fortilink-TS with TiPlus Technology Transforaminal/Posterior Lumbar Cage
TW: “百適”弗帝希腰椎系統椎間/後方腰椎融合裝置
Risk Class 2
MD

Registration Details

299bdd528d7b9b1363b46c143b728495

Ministry of Health Medical Device Import No. 036289

DHA05603628902

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

Jan 19, 2023

Jan 19, 2028