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"Stryker" ultrafine catheter - Taiwan Registration b68b91d837e6de26b43235aa28f49afe

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 b68b91d837e6de26b43235aa28f49afe 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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b68b91d837e6de26b43235aa28f49afe
Registration Details
Taiwan FDA Registration: b68b91d837e6de26b43235aa28f49afe
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Device Details

"Stryker" ultrafine catheter
TW: "ๅฒ่ณฝๅ…‹" ่ถ…ๅพฎ็ดฐๅฐŽ็ฎก
Risk Class 2

Registration Details

b68b91d837e6de26b43235aa28f49afe

DHA00601181200

Company Information

Ireland

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Sep 05, 2005

Sep 05, 2025

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