Pure Global

"Udek" Ines multi-branch stent graft system - Taiwan Registration 30194d597bbc8669f1f22fa1fced1e9a

Access comprehensive regulatory information for "Udek" Ines multi-branch 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 30194d597bbc8669f1f22fa1fced1e9a 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
30194d597bbc8669f1f22fa1fced1e9a
Registration Details
Taiwan FDA Registration: 30194d597bbc8669f1f22fa1fced1e9a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Udek" Ines multi-branch stent graft system
TW: โ€œๅ„ชๅพทๅ…‹โ€ ไผŠๆฉๆ–ฏๅคšๅˆ†ๆ”ฏ่ฆ†่†œๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

30194d597bbc8669f1f22fa1fced1e9a

DHA05603741509

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.0006.

import

Dates and Status

Sep 26, 2024

Sep 26, 2029