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“Zimmer” Persona Revision Knee System - Taiwan Registration bd5189f301914dc2c5a2fa6122ccaa9b

Access comprehensive regulatory information for “Zimmer” Persona Revision 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 bd5189f301914dc2c5a2fa6122ccaa9b 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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bd5189f301914dc2c5a2fa6122ccaa9b
Registration Details
Taiwan FDA Registration: bd5189f301914dc2c5a2fa6122ccaa9b
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Device Details

“Zimmer” Persona Revision Knee System
TW: “捷邁” 博適耐重建型全人工膝關節系統
Risk Class 2
MD

Registration Details

bd5189f301914dc2c5a2fa6122ccaa9b

Ministry of Health Medical Device Import No. 035929

DHA05603592904

Company Information

United States

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

Oct 07, 2022

Oct 07, 2027