"Stryker" Cardille Remote Guided Catheter - Taiwan Registration 9e2ea8b02b4f79f0e710905839c33b2f
Access comprehensive regulatory information for "Stryker" Cardille Remote Guided Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e2ea8b02b4f79f0e710905839c33b2f 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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9e2ea8b02b4f79f0e710905839c33b2f
Registration Details
Taiwan FDA Registration: 9e2ea8b02b4f79f0e710905839c33b2f
Device Details
"Stryker" Cardille Remote Guided Catheter
TW: โๅฒ่ณฝๅ
โๅกๅพๆจ้ ็ซฏๅผๅฐๅฐ็ฎก
Risk Class 2

