"Stryker" plastic ultrafine catheter - Taiwan Registration 696628de5cc012ded74c16f9f3895148
Access comprehensive regulatory information for "Stryker" plastic 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 696628de5cc012ded74c16f9f3895148 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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696628de5cc012ded74c16f9f3895148
Registration Details
Taiwan FDA Registration: 696628de5cc012ded74c16f9f3895148
Device Details
"Stryker" plastic ultrafine catheter
TW: "ๅฒ่ณฝๅ
" ๅกๅ่ถ
ๅพฎ็ดฐๅฐ็ฎก
Risk Class 2

