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"Stryker" microcatheter - Taiwan Registration 49f5bd82f2a1de430d22f9af4b08c3ec

Access comprehensive regulatory information for "Stryker" microcatheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49f5bd82f2a1de430d22f9af4b08c3ec 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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49f5bd82f2a1de430d22f9af4b08c3ec
Registration Details
Taiwan FDA Registration: 49f5bd82f2a1de430d22f9af4b08c3ec
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Device Details

"Stryker" microcatheter
TW: โ€œๅฒ่ณฝๅ…‹โ€ๅพฎๅฐŽ็ฎก
Risk Class 2

Registration Details

49f5bd82f2a1de430d22f9af4b08c3ec

DHA00602447401

Company Information

Ireland;;United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Feb 18, 2013

Feb 18, 2028