Taiwan FDA registration 3bf072a3b03adcd3724ecd6efd1f5752

"Arno" single-lumen central venous catheter group

TW: “亞諾”單腔中央靜脈導管組
Taiwan flagTaiwan·Risk Class 2·Arrow Internacional de Chihuahua S.A. de C.V.;; Arrow International LLC(Subsidiary of Teleflex Incorporated)·Registered Oct 13, 2016 – Oct 13, 2026Active
Registration details
Analysis ID
3bf072a3b03adcd3724ecd6efd1f5752
Customs Code
DHA05602898102
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
Input;; Contract manufacturing
Dates and status
Registration Date
Oct 13, 2016
Expiry Date
Oct 13, 2026
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About this record

Access comprehensive regulatory information for "Arno" single-lumen 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 3bf072a3b03adcd3724ecd6efd1f5752 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 International CR, a.s.;; Arrow International, Inc.(Subsidiary of Teleflex Inc.), 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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