"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.
Device Details
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
"Telifano" multi-lumen central venous catheter
ARROW INTERNATIONAL INC.
65979ed836368951f548c77646bc23f4
2
"Telifano" multi-lumen central venous catheter
Arrow International C.R. a.s.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)
0e37968c71bf569a11b6aba324663f06
2

