"Stryker" Zedent acetabular cup system - Taiwan Registration beffeda25584f299c7a6299d32939474
Access comprehensive regulatory information for "Stryker" Zedent acetabular cup system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number beffeda25584f299c7a6299d32939474 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.
Device Details
Registration Details
beffeda25584f299c7a6299d32939474
DHA00601029307
Product Details
N Orthopedics
N.3353 Semi-restricted Segment Joints of Metallic/Ceramic/Polymer-like Bone Cement or Non-Porous Coating Cement-free Cement-type Supplements
Contract manufacturing;; input
Dates and Status
May 07, 2003
May 07, 2028

