"Stryker" foot fixation system - Taiwan Registration b431a2d062178b744f9cce6b0c07f447
Access comprehensive regulatory information for "Stryker" foot fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b431a2d062178b744f9cce6b0c07f447 and manufactured by Stryker GmbH;; STRYKER LEIBINGER GMBH & CO. KG. 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.
Device Details
Registration Details
b431a2d062178b744f9cce6b0c07f447
DHA00602191207
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedics
N.3030 Single or multiple metallic bone fixation devices and accessories
import
Dates and Status
Jan 19, 2011
Jan 19, 2026

