Taiwan FDA registration 30b0c7e7042fda50564c5a3b921fe983

"Telifano" anti-infective pressure injection type peripherally placed in the central venous catheter group

TW: “泰利福亞諾” 抗感染壓力注射型週邊置入中央靜脈導管組
Taiwan flagTaiwan·Risk Class 2·Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated)·Registered Nov 09, 2021 – Nov 09, 2026Active
Registration details
Analysis ID
30b0c7e7042fda50564c5a3b921fe983
Customs Code
DHA05603502400
Company information
Manufacturer Country
Mexico;;United States
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5970 Percutaneous long-term implantable endovascular catheters
Import Information
import
Dates and status
Registration Date
Nov 09, 2021
Expiry Date
Nov 09, 2026
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About this record

Access comprehensive regulatory information for "Telifano" anti-infective pressure injection type peripherally placed in the central venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30b0c7e7042fda50564c5a3b921fe983 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, 1 companies making similar products including Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC (subsidiary of Teleflex Incorporated), and 1 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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