Taiwan FDA registration 9984f8af12206e7a9cd52ae0a74d3008
"Xinwei Medical" intracranial balloon dilation catheter
TW: “心瑋醫療” 顱內球囊擴張導管
Taiwan·Risk Class 2·Shanghai HeartCare Medical Technology Corporation Limited·Registered Jan 01, 2024 – Jan 01, 2029ActiveRegistration details
- Analysis ID
- 9984f8af12206e7a9cd52ae0a74d3008
- Customs Code
- DHA09200151304
Company information
- Manufacturer Country
- China
- Authorized Representative
- BUDDY MEDICAL 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.1250 Percutaneous catheters
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 01, 2024
- Expiry Date
- Jan 01, 2029
About this record
Access comprehensive regulatory information for "Xinwei Medical" intracranial balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9984f8af12206e7a9cd52ae0a74d3008 and manufactured by Shanghai HeartCare Medical Technology Corporation Limited. The authorized representative in Taiwan is BUDDY MEDICAL CO., LTD..
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