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“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.

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0c7d981001e2b5474dac8c296cb0e567
Registration Details
Taiwan FDA Registration: 0c7d981001e2b5474dac8c296cb0e567
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Device Details

“Stryker” Neuroform Atlas Stent System
TW: “史賽克”紐偌楓艾特斯支架系統
Risk Class 3
MD

Registration Details

0c7d981001e2b5474dac8c296cb0e567

Ministry of Health Medical Device Import No. 029356

DHA05602935600

Company Information

Ireland

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