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“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.

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c9c30d593c3837387221aa7ae2c03289
Registration Details
Taiwan FDA Registration: c9c30d593c3837387221aa7ae2c03289
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Device Details

“Stryker” Surpass Streamline Flow Diverter
TW: “史賽克”充沛流量導引器
Risk Class 3
MD
Cancelled

Registration Details

c9c30d593c3837387221aa7ae2c03289

Ministry of Health Medical Device Import No. 029622

DHA05602962205

Company Information

Ireland

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

Logged out

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