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"Stryker" Zedent second generation acetabular system - Taiwan Registration b1720c7f775137a6b3f2e8b519dd59de

Access comprehensive regulatory information for "Stryker" Zedent second generation 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 b1720c7f775137a6b3f2e8b519dd59de and manufactured by STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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b1720c7f775137a6b3f2e8b519dd59de
Registration Details
Taiwan FDA Registration: b1720c7f775137a6b3f2e8b519dd59de
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Device Details

"Stryker" Zedent second generation acetabular system
TW: โ€œๅฒ่ณฝๅ…‹โ€้‡‡็™ป็‰น็ฌฌไบŒไปฃ้ซ–่‡ผ็ณป็ตฑ
Risk Class 2

Registration Details

b1720c7f775137a6b3f2e8b519dd59de

DHA05603480201

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N.3358 Semi-restricted correlated metals/polymers/metals porous coating and cementless cement supplements

import

Dates and Status

Aug 01, 2021

Aug 01, 2026