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“Minvasys” StemiCath Thromboaspiration Catheter - Taiwan Registration 3d9a3b9a6d067b8d53920bb4d988adb3

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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3d9a3b9a6d067b8d53920bb4d988adb3
Registration Details
Taiwan FDA Registration: 3d9a3b9a6d067b8d53920bb4d988adb3
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Device Details

“Minvasys” StemiCath Thromboaspiration Catheter
TW: “尼瓦西斯”血栓吸除導管
Risk Class 2
MD

Registration Details

3d9a3b9a6d067b8d53920bb4d988adb3

Ministry of Health Medical Device Import No. 026209

DHA05602620908

Company Information

France

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E5150 Thrombectomy catheter

Imported from abroad

Dates and Status

May 22, 2014

May 22, 2024