Taiwan FDA registration e03f273df9acd6fbb7cd22ee61b1875e

"Telifano" multi-lumen hemodialysis catheter

TW: “泰利福亞諾”多腔血液透析導管
Taiwan flagTaiwan·Risk Class 2·Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)·Registered Jul 25, 2018 – Jul 25, 2023Expired
Registration details
Analysis ID
e03f273df9acd6fbb7cd22ee61b1875e
Customs Code
DHA05603136707
Company information
Manufacturer Country
United States;;Czechia
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5540 Blood Access Devices and Accessories
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jul 25, 2018
Expiry Date
Jul 25, 2023
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About this record

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 e03f273df9acd6fbb7cd22ee61b1875e 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, 1 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; 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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