Pure Global

"Telifano" multi-lumen central venous catheter - Taiwan Registration 65979ed836368951f548c77646bc23f4

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 65979ed836368951f548c77646bc23f4 and manufactured by ARROW INTERNATIONAL INC.. 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 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
2 Competitors
2 Recent Registrations
65979ed836368951f548c77646bc23f4
Registration Details
Taiwan FDA Registration: 65979ed836368951f548c77646bc23f4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Telifano" multi-lumen central venous catheter
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ๅคš่…”ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

65979ed836368951f548c77646bc23f4

DHA05603088906

Company Information

United States

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 02, 2018

May 02, 2023