“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.
Device Details
Registration Details
157627b0cfa207364286ae45a7b0fb59
Ministry of Health Medical Device Import No. 034623
DHA05603462301
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

