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"Stryker" Zeident second generation porous acetabular cup - Taiwan Registration 98eb3ec137eb905ce957ed58abc86b08

Access comprehensive regulatory information for "Stryker" Zeident second generation porous acetabular cup in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98eb3ec137eb905ce957ed58abc86b08 and manufactured by Made (部分製程) in FRANCE;; STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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98eb3ec137eb905ce957ed58abc86b08
Registration Details
Taiwan FDA Registration: 98eb3ec137eb905ce957ed58abc86b08
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Device Details

"Stryker" Zeident second generation porous acetabular cup
TW: “史賽克”采登特第二代多孔髖臼杯
Risk Class 2

Registration Details

98eb3ec137eb905ce957ed58abc86b08

DHA05603480405

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N.3353 Semi-restricted Segment Joints of Metallic/Ceramic/Polymer-like Bone Cement or Non-Porous Coating Cement-free Cement-type Supplements

import

Dates and Status

Aug 04, 2021

Aug 04, 2026