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Femur/condyle titanium alloy bone nail plate system - Taiwan Registration 3ac192a344ae2298e00566ff54c1e28f

Access comprehensive regulatory information for Femur/condyle titanium alloy bone nail plate system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 3ac192a344ae2298e00566ff54c1e28f and manufactured by STRYKER TRAUMA-SELZACH AG. 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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3ac192a344ae2298e00566ff54c1e28f
Registration Details
Taiwan FDA Registration: 3ac192a344ae2298e00566ff54c1e28f
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Device Details

Femur/condyle titanium alloy bone nail plate system
TW: ่‚ก้ชจ/้ซ้ชจ้ˆฆๅˆ้‡‘้ชจ้‡˜้ชจๆฟ็ณป็ตฑ
Cancelled

Registration Details

3ac192a344ae2298e00566ff54c1e28f

DHA00600922401

Company Information

Switzerland

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Jun 29, 1999

Feb 09, 2004

Jul 18, 2007

Cancellation Information

Logged out

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