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“Teleflex Arrow” Berman Angiographic Balloon Catheters - Taiwan Registration fd8176e6e359fd586a392ceecf9d254e

Access comprehensive regulatory information for “Teleflex Arrow” Berman Angiographic Balloon Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd8176e6e359fd586a392ceecf9d254e and manufactured by Arrow International, LLC (Subsidiary of Teleflex, Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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fd8176e6e359fd586a392ceecf9d254e
Registration Details
Taiwan FDA Registration: fd8176e6e359fd586a392ceecf9d254e
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Device Details

“Teleflex Arrow” Berman Angiographic Balloon Catheters
TW: “泰利福亞諾” 帕曼心血管造影導管
Risk Class 2
MD

Registration Details

fd8176e6e359fd586a392ceecf9d254e

Ministry of Health Medical Device Import No. 030813

DHA05603081302

Company Information

Product Details

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

E Cardiovascular devices

E1200 Diagnostic endovascular catheter

Imported from abroad

Dates and Status

Apr 22, 2018

Apr 22, 2023