Taiwan FDA registration b51b68d7269eaff7379f21fb91db982a
"UDEK" Itag stent graft system
TW: “優德克” 伊塔格覆膜支架系統
Registration details
- Analysis ID
- b51b68d7269eaff7379f21fb91db982a
- Customs Code
- DHA05603746804
Company information
- Manufacturer
- JOTEC GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Nov 26, 2024
- Expiry Date
- Nov 26, 2029
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices