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"Meiku" unilateral artificial knee tibial pad - Taiwan Registration ade09c093de9af8450b9a69ca1f864a0

Access comprehensive regulatory information for "Meiku" unilateral artificial knee tibial pad in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ade09c093de9af8450b9a69ca1f864a0 and manufactured by MAKO Surgical Corp.;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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ade09c093de9af8450b9a69ca1f864a0
Registration Details
Taiwan FDA Registration: ade09c093de9af8450b9a69ca1f864a0
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Device Details

"Meiku" unilateral artificial knee tibial pad
TW: โ€œ็พŽ้…ทโ€ๅ–ฎๅดไบบๅทฅ่†้—œ็ฏ€่„›้ชจๅ…งๅขŠ
Risk Class 2

Registration Details

ade09c093de9af8450b9a69ca1f864a0

DHA05603527407

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N.3520 Non-restrictive femoral tibial metal/polymer cemented remedy for knee joints

import

Dates and Status

Feb 23, 2022

Feb 23, 2027