Taiwan FDA registration 30194d597bbc8669f1f22fa1fced1e9a
"Udek" Ines multi-branch stent graft system
TW: “優德克” 伊恩斯多分支覆膜支架系統
Taiwan·Risk Class 3·Jotec GmbH·Registered Sep 26, 2024 – Sep 26, 2029ActiveRegistration details
- Analysis ID
- 30194d597bbc8669f1f22fa1fced1e9a
- Customs Code
- DHA05603741509
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.0006.
- Import Information
- import
Dates and status
- Registration Date
- Sep 26, 2024
- Expiry Date
- Sep 26, 2029
About this record
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.
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