“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.
Device Details
Registration Details
d18c667b946e0297a71b4e79420f7919
Ministry of Health Medical Device Import No. 034806
DHA05603480609
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

