Taiwan FDA registration b0c8fe7887a37d4b6ee119eb19ac6271
"Medtronic" Van Ren Dena Vion thoracic aortic stent system
TW: “美敦力”范倫特納威昂胸主動脈支架系統
Taiwan·Risk Class 3·MEDTRONIC IRELAND·Registered Jan 07, 2020 – Jan 07, 2025ExpiredRegistration details
- Analysis ID
- b0c8fe7887a37d4b6ee119eb19ac6271
- Customs Code
- DHA05603308609
Company information
- Manufacturer
- MEDTRONIC IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0006.
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Jan 07, 2020
- Expiry Date
- Jan 07, 2025
About this record
Access comprehensive regulatory information for "Medtronic" Van Ren Dena Vion thoracic aortic stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b0c8fe7887a37d4b6ee119eb19ac6271 and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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