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“Teleflex Arrow” ARROWgard Catheters - Taiwan Registration d3d4fc7e9607eb76c204872880ff12b1

Access comprehensive regulatory information for “Teleflex Arrow” ARROWgard Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3d4fc7e9607eb76c204872880ff12b1 and manufactured by ARROW INTERNATIONAL INC.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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d3d4fc7e9607eb76c204872880ff12b1
Registration Details
Taiwan FDA Registration: d3d4fc7e9607eb76c204872880ff12b1
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Device Details

“Teleflex Arrow” ARROWgard Catheters
TW: “泰利福亞諾”抗感染中央靜脈導管套組
Risk Class 2
MD

Registration Details

d3d4fc7e9607eb76c204872880ff12b1

Ministry of Health Medical Device Import No. 030806

DHA05603080602

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J5200 Intravascular catheter

Imported from abroad

Dates and Status

Apr 16, 2018

Apr 16, 2023