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“E-VITA” OPEN PLUS STENT GRAFT SYSTEM - Taiwan Registration 05b4d3e0951ef18ad7a52ed953b874a5

Access comprehensive regulatory information for “E-VITA” OPEN PLUS STENT GRAFT SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 05b4d3e0951ef18ad7a52ed953b874a5 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.

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05b4d3e0951ef18ad7a52ed953b874a5
Registration Details
Taiwan FDA Registration: 05b4d3e0951ef18ad7a52ed953b874a5
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Device Details

“E-VITA” OPEN PLUS STENT GRAFT SYSTEM
TW: “依威達”開放加強式血管支架系統
Risk Class 3
MD
Cancelled

Registration Details

05b4d3e0951ef18ad7a52ed953b874a5

Ministry of Health Medical Device Import No. 026306

DHA05602630606

Company Information

Germany

Product Details

E Cardiovascular devices

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Dec 10, 2014

Dec 10, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者