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“Smith & Nephew” Journey II TKA Total Knee System - Taiwan Registration 25a4d19ccc40984f87c749f0542a4771

Access comprehensive regulatory information for “Smith & Nephew” Journey II TKA Total Knee System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25a4d19ccc40984f87c749f0542a4771 and manufactured by Smith & Nephew, Inc.. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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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25a4d19ccc40984f87c749f0542a4771
Registration Details
Taiwan FDA Registration: 25a4d19ccc40984f87c749f0542a4771
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Device Details

“Smith & Nephew” Journey II TKA Total Knee System
TW: “史耐輝”全膝關節系統
Risk Class 2
MD

Registration Details

25a4d19ccc40984f87c749f0542a4771

Ministry of Health Medical Device Import No. 036489

DHA05603648907

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3560 Semi-restrictive knee femoral tibial polymer/metal/polymeric cement compound

Imported from abroad

Dates and Status

May 01, 2023

May 01, 2028