"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.
Device Details
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
"Telifano" multi-lumen central venous catheter
ARROW INTERNATIONAL INC.
65979ed836368951f548c77646bc23f4
2
"Telifano" multi-lumen central venous catheter
Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated)
f98a32b8f9151e36672ea63bb2aaa27e
2

