Taiwan FDA registration f264893b9be6bc4354e66a892964cbc0
“Edwards” Carpentier-Edwards PERIMOUNT Pericardial Bioprosthesis
TW: “愛德華” 卡本特-愛德華沛旅旺心包生物瓣膜
Taiwan·Risk Class 3·MD·EDWARDS LIFESCIENCES LLC·Registered Aug 26, 2013 – Aug 26, 2028ActiveRegistration details
- Analysis ID
- f264893b9be6bc4354e66a892964cbc0
- License Form
- Ministry of Health Medical Device Import No. 025232
- Customs Code
- DHA05602523201
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 devices
- Product Type (Level 2)
- E3925 Heart valve replacement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 26, 2013
- Expiry Date
- Aug 26, 2028
About this record
Access comprehensive regulatory information for “Edwards” Carpentier-Edwards PERIMOUNT Pericardial Bioprosthesis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f264893b9be6bc4354e66a892964cbc0 and manufactured by EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.
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