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“Stryker” Distal Access Catheter - Taiwan Registration f153e980f56d7f5846a1cbb40b1d86c4

Access comprehensive regulatory information for “Stryker” Distal Access Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f153e980f56d7f5846a1cbb40b1d86c4 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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f153e980f56d7f5846a1cbb40b1d86c4
Registration Details
Taiwan FDA Registration: f153e980f56d7f5846a1cbb40b1d86c4
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Device Details

“Stryker” Distal Access Catheter
TW: “史賽克”遠端輔助導管
Risk Class 2
MD
Cancelled

Registration Details

f153e980f56d7f5846a1cbb40b1d86c4

Ministry of Health Medical Device Import No. 026678

DHA05602667804

Company Information

United States

Product Details

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Nov 17, 2014

Nov 17, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者