"Stryker" femoral head - Taiwan Registration 92d7b12a5ee178f87be4a525960b6ec7
Access comprehensive regulatory information for "Stryker" femoral head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92d7b12a5ee178f87be4a525960b6ec7 and manufactured by STRYKER IRELAND LIMITED;; HOWMEDICA OSTEONICS CORP.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOWMEDICA OSTEONICS-STRYKER IRELAND, and 1 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
92d7b12a5ee178f87be4a525960b6ec7
DHA05602970101
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedics
N.3350 Semi-restricted cormium/polymer-like cement-type supplements
Input;; Contract manufacturing
Dates and Status
Apr 26, 2017
Apr 26, 2027

