“Stryker” Neuroform Atlas Stent System - Taiwan Registration 0c7d981001e2b5474dac8c296cb0e567
Access comprehensive regulatory information for “Stryker” Neuroform Atlas Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c7d981001e2b5474dac8c296cb0e567 and manufactured by Stryker Neurovascular. 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
0c7d981001e2b5474dac8c296cb0e567
Ministry of Health Medical Device Import No. 029356
DHA05602935600
Product Details
For details, it is Chinese approved copy of the imitation order
K Devices for neuroscience
K5950 Artificial embolization device
Imported from abroad
Dates and Status
Jan 26, 2017
Jan 26, 2027

