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“Centinel Spine” MIDLINE II-TI - Taiwan Registration c455a6c6825e1dcad4e8a44901c56172

Access comprehensive regulatory information for “Centinel Spine” MIDLINE II-TI in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c455a6c6825e1dcad4e8a44901c56172 and manufactured by Centinel Spine, LLC. The authorized representative in Taiwan is RACK MEDICAL TECHNOLOGIES, INC..

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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c455a6c6825e1dcad4e8a44901c56172
Registration Details
Taiwan FDA Registration: c455a6c6825e1dcad4e8a44901c56172
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Device Details

“Centinel Spine” MIDLINE II-TI
TW: “伸特耐-脊椎”美特耐腰椎椎間融合器
Risk Class 2
MD

Registration Details

c455a6c6825e1dcad4e8a44901c56172

Ministry of Health Medical Device Import No. 035070

DHA05603507004

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

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Imported from abroad

Dates and Status

Nov 28, 2021

Nov 28, 2026