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"Telifano" multi-lumen central venous catheter - Taiwan Registration 0e37968c71bf569a11b6aba324663f06

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 0e37968c71bf569a11b6aba324663f06 and manufactured by Arrow International C.R. a.s.;; 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 Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), ARROW INTERNATIONAL INC., 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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0e37968c71bf569a11b6aba324663f06
Registration Details
Taiwan FDA Registration: 0e37968c71bf569a11b6aba324663f06
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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

0e37968c71bf569a11b6aba324663f06

DHA05603088307

Product Details

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

J General hospital and personal use equipment

J.5200 Endovascular catheters

Input;; Contract manufacturing

Dates and Status

May 01, 2018

May 01, 2023