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"Telifano" multi-lumen hemodialysis catheter - Taiwan Registration 5c03b2ea5e2b938bff11c764bd1a5700

Access comprehensive regulatory information for "Telifano" multi-lumen hemodialysis catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c03b2ea5e2b938bff11c764bd1a5700 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, 1 companies making similar products including Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated), and 1 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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5c03b2ea5e2b938bff11c764bd1a5700
Registration Details
Taiwan FDA Registration: 5c03b2ea5e2b938bff11c764bd1a5700
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Device Details

"Telifano" multi-lumen hemodialysis catheter
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ๅคš่…”่ก€ๆถฒ้€ๆžๅฐŽ็ฎก
Risk Class 2

Registration Details

5c03b2ea5e2b938bff11c764bd1a5700

DHA05603104804

Product Details

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

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

import

Dates and Status

Apr 23, 2018

Apr 23, 2023

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