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"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
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Device Details

"Xenex" Meidex femoral arteriovenous catheter
TW: โ€œ่ณฝ่€ๅธโ€็พŽๅพทๆ€่‚กๅ‹•้œ่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

2a1b0ad4ed0d3a3eaa2e2567b34372fa

DHA00601855308

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Jan 18, 2008

Jan 18, 2028