Taiwan FDA registration 3d9a3b9a6d067b8d53920bb4d988adb3
“Minvasys” StemiCath Thromboaspiration Catheter
TW: “尼瓦西斯”血栓吸除導管
Taiwan·Risk Class 2·MD·MINVASYS·Registered May 22, 2014 – May 22, 2024ExpiredRegistration details
- Analysis ID
- 3d9a3b9a6d067b8d53920bb4d988adb3
- License Form
- Ministry of Health Medical Device Import No. 026209
- Customs Code
- DHA05602620908
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)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 22, 2014
- Expiry Date
- May 22, 2024
About this record
Access comprehensive regulatory information for “Minvasys” StemiCath Thromboaspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d9a3b9a6d067b8d53920bb4d988adb3 and manufactured by MINVASYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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