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"Xenex" Meidex Tubing Group - Taiwan Registration 72ea7eb8e49f364fdd6e893daa0cfa50

Access comprehensive regulatory information for "Xenex" Meidex Tubing Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72ea7eb8e49f364fdd6e893daa0cfa50 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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72ea7eb8e49f364fdd6e893daa0cfa50
Registration Details
Taiwan FDA Registration: 72ea7eb8e49f364fdd6e893daa0cfa50
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Device Details

"Xenex" Meidex Tubing Group
TW: โ€œ่ณฝ่€ๅธโ€ ็พŽๅพทๆ€็ฎก่ทฏ็ต„
Risk Class 2

Registration Details

72ea7eb8e49f364fdd6e893daa0cfa50

DHA00602206500

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

Input;; Contract manufacturing

Dates and Status

Feb 21, 2011

Feb 21, 2026