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"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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c0c8a85cc7500ecaa0b2ff167241df81
Registration Details
Taiwan FDA Registration: c0c8a85cc7500ecaa0b2ff167241df81
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Device Details

"Stryker" artificial tibial inner pad system
TW: "ๅฒ่ณฝๅ…‹"ไบบๅทฅ่„›้ชจๅ…งๅขŠ็ณป็ตฑ
Risk Class 2

Registration Details

c0c8a85cc7500ecaa0b2ff167241df81

DHA00601698300

Company Information

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