"Stryker" hand bone plate system - Taiwan Registration d5f431e2702ccbc6705870ee63661378
Access comprehensive regulatory information for "Stryker" hand bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5f431e2702ccbc6705870ee63661378 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
d5f431e2702ccbc6705870ee63661378
DHA00601951202
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
Dec 18, 2008
Dec 18, 2028

