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“Stryker” Surpass Evolve Flow Diverter System - Taiwan Registration 1e73d80a4efe18113683ca61a2b8fcd9

Access comprehensive regulatory information for “Stryker” Surpass Evolve Flow Diverter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1e73d80a4efe18113683ca61a2b8fcd9 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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1e73d80a4efe18113683ca61a2b8fcd9
Registration Details
Taiwan FDA Registration: 1e73d80a4efe18113683ca61a2b8fcd9
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Device Details

“Stryker” Surpass Evolve Flow Diverter System
TW: “史賽克”充沛流量導引套
Risk Class 3
MD

Registration Details

1e73d80a4efe18113683ca61a2b8fcd9

Ministry of Health Medical Device Import No. 034283

DHA05603428303

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

Feb 06, 2021

Feb 06, 2026