"Stryker" clinical sample (unsterilized) - Taiwan Registration ea65abc9e5ff0b86dc99526e81658baa
Access comprehensive regulatory information for "Stryker" clinical sample (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ea65abc9e5ff0b86dc99526e81658baa and manufactured by ORTHOVITA INC.;; 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, 4 companies making similar products including STRYKER GMBH, LISI MEDICAL ORTHOPAEDICS;; HOWMEDICA OSTEONICS CORP., and 4 recent registrations in the same category. 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
ea65abc9e5ff0b86dc99526e81658baa
DHA04401160907
Product Details
Limited to the first level identification range of the "clinical use model (N.4800)" of the Measures for the Administration of Medical Devices.
N Orthopedics
N.4800 Sample plate for clinical use
import
Dates and Status
Apr 18, 2012
Apr 18, 2022
Apr 12, 2024
Cancellation Information
Logged out
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