Taiwan FDA registration 4c2567de5b42705c1716b107e6c80d5f
"Decant Flex" aortic stent system
TW: “潷葛睿孚”主動脈覆膜支架系統
Taiwan·Risk Class 3·Bentley InnoMed GmbH·Registered Feb 12, 2020 – Feb 12, 2030ActiveRegistration details
- Analysis ID
- 4c2567de5b42705c1716b107e6c80d5f
- Customs Code
- DHA05603325200
Company information
- Manufacturer
- Bentley InnoMed GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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
- import
Dates and status
- Registration Date
- Feb 12, 2020
- Expiry Date
- Feb 12, 2030
About this record
Access comprehensive regulatory information for "Decant Flex" 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 4c2567de5b42705c1716b107e6c80d5f and manufactured by Bentley InnoMed GmbH. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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