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"Telifano" single-lumen central venous catheter - Taiwan Registration ed8caeae5e14c5840b881561fc436eac

Access comprehensive regulatory information for "Telifano" single-lumen central venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed8caeae5e14c5840b881561fc436eac and manufactured by Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

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ed8caeae5e14c5840b881561fc436eac
Registration Details
Taiwan FDA Registration: ed8caeae5e14c5840b881561fc436eac
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Device Details

"Telifano" single-lumen central venous catheter
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ๅ–ฎ่…”ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

ed8caeae5e14c5840b881561fc436eac

DHA05603088804

Product Details

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

J General hospital and personal use equipment

J.5200 Endovascular catheters

import

Dates and Status

May 02, 2018

May 02, 2023