“Stryker” Surpass Streamline Flow Diverter - Taiwan Registration c9c30d593c3837387221aa7ae2c03289
Access comprehensive regulatory information for “Stryker” Surpass Streamline Flow Diverter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c9c30d593c3837387221aa7ae2c03289 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
c9c30d593c3837387221aa7ae2c03289
Ministry of Health Medical Device Import No. 029622
DHA05602962205
Product Details
K Devices for neuroscience
K5950 Artificial embolization device
Imported from abroad
Dates and Status
Apr 05, 2017
Apr 05, 2022
May 23, 2022
Cancellation Information
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