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"Goodeka Osdenin" Skobio classic all-artificial knee system - Taiwan Registration 4b8b67e97bf5ba38164f3f376bf205b6

Access comprehensive regulatory information for "Goodeka Osdenin" Skobio classic all-artificial knee system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b8b67e97bf5ba38164f3f376bf205b6 and manufactured by 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.

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4b8b67e97bf5ba38164f3f376bf205b6
Registration Details
Taiwan FDA Registration: 4b8b67e97bf5ba38164f3f376bf205b6
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Device Details

"Goodeka Osdenin" Skobio classic all-artificial knee system
TW: โ€œๅฅฝ็พŽๅพ—ๅก-ๅฅงๆ–ฏๅพ—ๅฏงโ€ๆ–ฏ้ซ˜ๆฏ”ๆญ็ถ“ๅ…ธๅ…จไบบๅทฅ่†้—œ็ฏ€็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

4b8b67e97bf5ba38164f3f376bf205b6

DHA00602237601

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3565 Knee jointsFemoral metals/polymersPorous coatings of cementless cement

import

Dates and Status

May 09, 2011

May 09, 2021

Aug 17, 2023

Cancellation Information

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