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"Stryker" ultrafine catheter - Taiwan Registration 612b9c2a13d6216c44cf248c2aeba2d1

Access comprehensive regulatory information for "Stryker" ultrafine catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 612b9c2a13d6216c44cf248c2aeba2d1 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, 1 companies making similar products including Stryker Neurovascular, and 1 recent registrations in the same category. 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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612b9c2a13d6216c44cf248c2aeba2d1
Registration Details
Taiwan FDA Registration: 612b9c2a13d6216c44cf248c2aeba2d1
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Device Details

"Stryker" ultrafine catheter
TW: โ€œๅฒ่ณฝๅ…‹โ€่ถ…ๅพฎ็ดฐๅฐŽ็ฎก
Risk Class 2

Registration Details

612b9c2a13d6216c44cf248c2aeba2d1

DHA05603029707

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

Oct 25, 2017

Oct 25, 2027

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