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“Creagh” Tersus PTA Balloon Dilation Catheter - Taiwan Registration 72a0ab59a8b9916a0f0c6b4962a89a39

Access comprehensive regulatory information for “Creagh” Tersus PTA Balloon Dilation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72a0ab59a8b9916a0f0c6b4962a89a39 and manufactured by Creagh Medical Ltd.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..

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72a0ab59a8b9916a0f0c6b4962a89a39
Registration Details
Taiwan FDA Registration: 72a0ab59a8b9916a0f0c6b4962a89a39
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Device Details

“Creagh” Tersus PTA Balloon Dilation Catheter
TW: “克雷”特瑟斯周邊血管擴張術氣球導管
Risk Class 2
MD

Registration Details

72a0ab59a8b9916a0f0c6b4962a89a39

Ministry of Health Medical Device Import No. 028541

DHA05602854100

Company Information

Ireland

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

May 25, 2016

May 25, 2021