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"Telifano" multi-lumen central venous catheter - Taiwan Registration f98a32b8f9151e36672ea63bb2aaa27e

Access comprehensive regulatory information for "Telifano" multi-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 f98a32b8f9151e36672ea63bb2aaa27e 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..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including ARROW INTERNATIONAL INC., Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated), and 2 recent registrations in the same category. 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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f98a32b8f9151e36672ea63bb2aaa27e
Registration Details
Taiwan FDA Registration: f98a32b8f9151e36672ea63bb2aaa27e
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Device Details

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

Registration Details

f98a32b8f9151e36672ea63bb2aaa27e

DHA05603088409

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 01, 2018

May 01, 2023