Taiwan FDA registration 0fe0d6510365704491357f9f43ea7576
“MINVASYS” Yangtze PTCA Balloon Dilatation Catheter
TW: “尼瓦西斯”楊子冠狀動脈氣球擴張導管
Taiwan·Risk Class 2·MD·MINVASYS·Registered Feb 01, 2019 – Feb 01, 2024ExpiredRegistration details
- Analysis ID
- 0fe0d6510365704491357f9f43ea7576
- License Form
- Ministry of Health Medical Device Import No. 032103
- Customs Code
- DHA05603210304
Company information
- Manufacturer
- MINVASYS
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
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)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 01, 2019
- Expiry Date
- Feb 01, 2024
About this record
Access comprehensive regulatory information for “MINVASYS” Yangtze PTCA Balloon Dilatation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0fe0d6510365704491357f9f43ea7576 and manufactured by MINVASYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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