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“HEXACATH” RayFlow Multipurpose Infusion Catheter - Taiwan Registration 43390b0fb53cd95db90f5c9e22a19f64

Access comprehensive regulatory information for “HEXACATH” RayFlow Multipurpose Infusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43390b0fb53cd95db90f5c9e22a19f64 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..

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43390b0fb53cd95db90f5c9e22a19f64
Registration Details
Taiwan FDA Registration: 43390b0fb53cd95db90f5c9e22a19f64
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Device Details

“HEXACATH” RayFlow Multipurpose Infusion Catheter
TW: “海斯凱”瑞菲多功能灌注導管
Risk Class 2
MD

Registration Details

43390b0fb53cd95db90f5c9e22a19f64

Ministry of Health Medical Device Import No. 033808

DHA05603380808

Company Information

France

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Jul 07, 2020

Jul 07, 2025