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“TERSUS” 0.035” PTA Balloon Dilatation Catheter - Taiwan Registration fa6b7eb7d18ba0cbf6b9930432914aea

Access comprehensive regulatory information for “TERSUS” 0.035” PTA 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 fa6b7eb7d18ba0cbf6b9930432914aea and manufactured by Creagh Medical Ltd.. The authorized representative in Taiwan is JRV GLOBAL PARTNERS, LIMITED TAIWAN BRANCH (B.V.I).

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fa6b7eb7d18ba0cbf6b9930432914aea
Registration Details
Taiwan FDA Registration: fa6b7eb7d18ba0cbf6b9930432914aea
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Device Details

“TERSUS” 0.035” PTA Balloon Dilatation Catheter
TW: “泰速-35”氣球擴張導管
Risk Class 2
MD
Cancelled

Registration Details

fa6b7eb7d18ba0cbf6b9930432914aea

Ministry of Health Medical Device Import No. 029958

DHA05602995802

Company Information

Product Details

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Jul 07, 2017

Jul 07, 2022

Sep 22, 2023

Cancellation Information

Logged out

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