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“Teleflex Arrow” Intra-Aortic Balloon Catheters - Taiwan Registration c24a5e4dbd0b6e10d1eb2c4ba56d2cc4

Access comprehensive regulatory information for “Teleflex Arrow” Intra-Aortic Balloon Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c24a5e4dbd0b6e10d1eb2c4ba56d2cc4 and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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c24a5e4dbd0b6e10d1eb2c4ba56d2cc4
Registration Details
Taiwan FDA Registration: c24a5e4dbd0b6e10d1eb2c4ba56d2cc4
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Device Details

“Teleflex Arrow” Intra-Aortic Balloon Catheters
TW: “泰利福亞諾”主動脈球囊導管
Risk Class 3
MD

Registration Details

c24a5e4dbd0b6e10d1eb2c4ba56d2cc4

Ministry of Health Medical Device Import No. 031220

DHA05603122003

Company Information

United States

Product Details

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

E Cardiovascular devices

E3535 Control system for balloon dilation and control in the aortic arch

Imported from abroad

Dates and Status

Jul 22, 2018

Jul 22, 2023