Taiwan FDA registration f98a32b8f9151e36672ea63bb2aaa27e

"Telifano" multi-lumen central venous catheter

TW: “泰利福亞諾”多腔中央靜脈導管
Taiwan flagTaiwan·Risk Class 2·Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated)·Registered May 01, 2018 – May 01, 2023Expired
Registration details
Analysis ID
f98a32b8f9151e36672ea63bb2aaa27e
Customs Code
DHA05603088409
Company information
Manufacturer Country
Mexico;;United States
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)
J General hospital and personal use equipment
Product Type (Level 2)
J.5200 Endovascular catheters
Import Information
import
Dates and status
Registration Date
May 01, 2018
Expiry Date
May 01, 2023
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About this record

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.

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