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“Zimmer Biomet Spine” Zyston Spacer System - Taiwan Registration 92607ab9b1366feb60238bb0bf8b575f

Access comprehensive regulatory information for “Zimmer Biomet Spine” Zyston Spacer System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92607ab9b1366feb60238bb0bf8b575f and manufactured by ZIMMER BIOMET SPINE, INC.. The authorized representative in Taiwan is ZimVie 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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92607ab9b1366feb60238bb0bf8b575f
Registration Details
Taiwan FDA Registration: 92607ab9b1366feb60238bb0bf8b575f
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Device Details

“Zimmer Biomet Spine” Zyston Spacer System
TW: “捷邁”捷適登椎間穩定系統
Risk Class 2
MD

Registration Details

92607ab9b1366feb60238bb0bf8b575f

Ministry of Health Medical Device Import No. 031066

DHA05603106606

Company Information

United States

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

May 08, 2018

May 08, 2028