“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.
Device Details
Registration Details
e50bb837fd539ba0feb0909b6aa00250
Ministry of Health Medical Device Import No. 034340
DHA05603434002
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

