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“HumanTech” TRISTAN Cervical Interbody Fusion - Taiwan Registration d18c667b946e0297a71b4e79420f7919

Access comprehensive regulatory information for “HumanTech” TRISTAN Cervical Interbody Fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d18c667b946e0297a71b4e79420f7919 and manufactured by HumanTech Spine GmbH. The authorized representative in Taiwan is LI MIN BIOTECH CO., 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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d18c667b946e0297a71b4e79420f7919
Registration Details
Taiwan FDA Registration: d18c667b946e0297a71b4e79420f7919
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Device Details

“HumanTech” TRISTAN Cervical Interbody Fusion
TW: “優門鐵克”特利斯坦頸椎椎間融合器
Risk Class 2
MD

Registration Details

d18c667b946e0297a71b4e79420f7919

Ministry of Health Medical Device Import No. 034806

DHA05603480609

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Aug 04, 2021

Aug 04, 2026