"Xenex" Meidex femoral arteriovenous catheter - Taiwan Registration 2a1b0ad4ed0d3a3eaa2e2567b34372fa
Access comprehensive regulatory information for "Xenex" Meidex femoral arteriovenous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a1b0ad4ed0d3a3eaa2e2567b34372fa and manufactured by Xenios AG. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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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2a1b0ad4ed0d3a3eaa2e2567b34372fa
Registration Details
Taiwan FDA Registration: 2a1b0ad4ed0d3a3eaa2e2567b34372fa
Device Details
"Xenex" Meidex femoral arteriovenous catheter
TW: โ่ณฝ่ๅธโ็พๅพทๆ่กๅ้่ๅฐ็ฎก
Risk Class 2

