Taiwan FDA registration b0e520aafbdad80369953bd730bb35bd
"Serucon" coronary angioplasty balloon catheter
TW: “瑟璐潯”冠狀動脈成形術球囊導管
Taiwan·Risk Class 2·MedAlliance LLC;; MedAlliance CardioVascular SA·Registered Sep 17, 2022 – Sep 17, 2027ActiveRegistration details
- Analysis ID
- b0e520aafbdad80369953bd730bb35bd
- Customs Code
- DHA05603579407
Company information
- Manufacturer
- MedAlliance LLC;; MedAlliance CardioVascular SA
- Manufacturer Country
- United States;;Switzerland
- Authorized Representative
- REGISTAR CO., LTD.
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.0005.
- Import Information
- import
Dates and status
- Registration Date
- Sep 17, 2022
- Expiry Date
- Sep 17, 2027
About this record
Access comprehensive regulatory information for "Serucon" coronary angioplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0e520aafbdad80369953bd730bb35bd and manufactured by MedAlliance LLC;; MedAlliance CardioVascular SA. The authorized representative in Taiwan is REGISTAR CO., LTD..
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