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“Zimmer” Trilogy Acetabular System - Taiwan Registration 22992c1e39833eae9d0b19d4f0bae221

Access comprehensive regulatory information for “Zimmer” Trilogy Acetabular System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22992c1e39833eae9d0b19d4f0bae221 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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22992c1e39833eae9d0b19d4f0bae221
Registration Details
Taiwan FDA Registration: 22992c1e39833eae9d0b19d4f0bae221
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Device Details

“Zimmer” Trilogy Acetabular System
TW: “捷邁”人工髖關節臼杯
Risk Class 2
MD

Registration Details

22992c1e39833eae9d0b19d4f0bae221

Ministry of Health Medical Device Import No. 025775

DHA05602577500

Company Information

United States

Product Details

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

N Orthopedic devices

N3350 Semi-restricted hip metal/polymer cement compound

Imported from abroad

Dates and Status

Jan 29, 2014

Jan 29, 2029