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“Jotec”E-vita OPEN NEO - Taiwan Registration 157627b0cfa207364286ae45a7b0fb59

Access comprehensive regulatory information for “Jotec”E-vita OPEN NEO in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 157627b0cfa207364286ae45a7b0fb59 and manufactured by Jotec GmbH. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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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157627b0cfa207364286ae45a7b0fb59
Registration Details
Taiwan FDA Registration: 157627b0cfa207364286ae45a7b0fb59
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Device Details

“Jotec”E-vita OPEN NEO
TW: “優德克”伊維塔開放式血管支架系統
Risk Class 3
MD

Registration Details

157627b0cfa207364286ae45a7b0fb59

Ministry of Health Medical Device Import No. 034623

DHA05603462301

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Sep 05, 2022

Sep 05, 2027