Taiwan FDA registration 17f1a18c026e3d8b83d230b5e0978dca
"Edward" Sepion transcatheter heart valve and femoral cannula group
TW: “愛德華”瑟皮恩經導管心臟瓣膜及股動脈套管組
Taiwan·Risk Class 3·EDWARDS LIFESCIENCES LLC·Registered Nov 13, 2015 – Nov 13, 2025ExpiredRegistration details
- Analysis ID
- 17f1a18c026e3d8b83d230b5e0978dca
- Customs Code
- DHA05602798607
Company information
- Manufacturer
- EDWARDS LIFESCIENCES LLC
- Manufacturer Country
- United States
- Authorized Representative
- EDWARDS LIFESCIENCES (TAIWAN) CORPORATION
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.3925 Hypocardial membrane substitutions
- Import Information
- Safety monitoring;; import
Dates and status
- Registration Date
- Nov 13, 2015
- Expiry Date
- Nov 13, 2025
About this record
Access comprehensive regulatory information for "Edward" Sepion transcatheter heart valve and femoral cannula group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 17f1a18c026e3d8b83d230b5e0978dca and manufactured by EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.
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