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“Jotec” E-wire Guide Wire - Taiwan Registration e50bb837fd539ba0feb0909b6aa00250

Access comprehensive regulatory information for “Jotec” 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 e50bb837fd539ba0feb0909b6aa00250 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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e50bb837fd539ba0feb0909b6aa00250
Registration Details
Taiwan FDA Registration: e50bb837fd539ba0feb0909b6aa00250
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Device Details

“Jotec” E-wire Guide Wire
TW: “優德克” 伊旺導引線
Risk Class 2
MD

Registration Details

e50bb837fd539ba0feb0909b6aa00250

Ministry of Health Medical Device Import No. 034340

DHA05603434002

Company Information

Germany

Product Details

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

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Feb 23, 2021

Feb 23, 2026