Taiwan FDA registration 3751e52b2b3242f924c99d9b87ab4134

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

TW: “泰利福亞諾” 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 Jan 13, 2021 – Jan 13, 2026Expired
Registration details
Analysis ID
3751e52b2b3242f924c99d9b87ab4134
Customs Code
DHA05603430401
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.5970 Percutaneous long-term implantable endovascular catheters
Import Information
import
Dates and status
Registration Date
Jan 13, 2021
Expiry Date
Jan 13, 2026
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About this record

Access comprehensive regulatory information for "Telifano" 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 3751e52b2b3242f924c99d9b87ab4134 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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