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"Stryker" artificial femur - Taiwan Registration ecd4ca5301c57c896eee891e1011db4e

Access comprehensive regulatory information for "Stryker" artificial femur in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ecd4ca5301c57c896eee891e1011db4e and manufactured by STRYKER IRELAND LIMITED. 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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ecd4ca5301c57c896eee891e1011db4e
Registration Details
Taiwan FDA Registration: ecd4ca5301c57c896eee891e1011db4e
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Device Details

"Stryker" artificial femur
TW: "ๅฒ่ณฝๅ…‹" ไบบๅทฅ่‚ก้ชจ
Risk Class 2
Cancelled

Registration Details

ecd4ca5301c57c896eee891e1011db4e

DHA00600921500

Company Information

Ireland

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Jun 25, 1999

Aug 02, 2021

Sep 18, 2023

Cancellation Information

Logged out

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