"Stryker" artificial tibial inner pad system - Taiwan Registration c0c8a85cc7500ecaa0b2ff167241df81
Access comprehensive regulatory information for "Stryker" artificial tibial inner pad system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0c8a85cc7500ecaa0b2ff167241df81 and manufactured by 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
c0c8a85cc7500ecaa0b2ff167241df81
DHA00601698300
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedics
N.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers
import
Dates and Status
Aug 10, 2006
Aug 10, 2026

