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“Zimmer” Unicompartmental Knee System - Taiwan Registration a1228d0e0b013b2ac14701acb7ef9b28

Access comprehensive regulatory information for “Zimmer” Unicompartmental 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 a1228d0e0b013b2ac14701acb7ef9b28 and manufactured by ZIMMER,INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN 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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a1228d0e0b013b2ac14701acb7ef9b28
Registration Details
Taiwan FDA Registration: a1228d0e0b013b2ac14701acb7ef9b28
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Device Details

“Zimmer” Unicompartmental Knee System
TW: “捷邁”單側人工膝關節系統
Risk Class 2
MD

Registration Details

a1228d0e0b013b2ac14701acb7ef9b28

Ministry of Health Medical Device Import No. 025752

DHA05602575201

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3520 Unrestricted knee tibial metal/polymer cement compound

Imported from abroad

Dates and Status

Jan 07, 2014

Jan 07, 2029