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"UDEK" Itag stent graft system - Taiwan Registration b51b68d7269eaff7379f21fb91db982a

Access comprehensive regulatory information for "UDEK" Itag 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 b51b68d7269eaff7379f21fb91db982a 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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b51b68d7269eaff7379f21fb91db982a
Registration Details
Taiwan FDA Registration: b51b68d7269eaff7379f21fb91db982a
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Device Details

"UDEK" Itag stent graft system
TW: โ€œๅ„ชๅพทๅ…‹โ€ ไผŠๅก”ๆ ผ่ฆ†่†œๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

b51b68d7269eaff7379f21fb91db982a

DHA05603746804

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.0001 Cardiovascular stents

import

Dates and Status

Nov 26, 2024

Nov 26, 2029