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"Arno" single-lumen central venous catheter group - Taiwan Registration 3bf072a3b03adcd3724ecd6efd1f5752

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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3bf072a3b03adcd3724ecd6efd1f5752
Registration Details
Taiwan FDA Registration: 3bf072a3b03adcd3724ecd6efd1f5752
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Device Details

"Arno" single-lumen central venous catheter group
TW: โ€œไบž่ซพโ€ๅ–ฎ่…”ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

3bf072a3b03adcd3724ecd6efd1f5752

DHA05602898102

Product Details

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

J General hospital and personal use equipment

J.5200 Endovascular catheters

Input;; Contract manufacturing

Dates and Status

Oct 13, 2016

Oct 13, 2026

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