“E-WIRE” GUIDE WIRE - Taiwan Registration 8632d5ca615b72bcc7bbd139da4de3ca

Access comprehensive regulatory information for “E-WIRE” GUIDE WIRE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8632d5ca615b72bcc7bbd139da4de3ca and manufactured by JOTEC GmbH. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..

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.