Pure Global

"Telifano" anti-infective central venous catheter sleeve - Taiwan Registration 486f924f1d0c89aa2d6a7c048c1cd91a

Access comprehensive regulatory information for "Telifano" anti-infective central venous catheter sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 486f924f1d0c89aa2d6a7c048c1cd91a 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. 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
486f924f1d0c89aa2d6a7c048c1cd91a
Registration Details
Taiwan FDA Registration: 486f924f1d0c89aa2d6a7c048c1cd91a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Telifano" anti-infective central venous catheter sleeve
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ ๆŠ—ๆ„ŸๆŸ“ไธญๅคฎ้œ่„ˆๅฐŽ็ฎกๅฅ—็ต„
Risk Class 2

Registration Details

486f924f1d0c89aa2d6a7c048c1cd91a

DHA05603080704

Product Details

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

J General hospital and personal use equipment

J.5200 Endovascular catheters

Contract manufacturing;; input

Dates and Status

Apr 16, 2018

Apr 16, 2023