"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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Device Details
Registration Details
98eb3ec137eb905ce957ed58abc86b08
DHA05603480405
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

