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"Telifano" pressure injection type peripherally placed in the central venous catheter group - Taiwan Registration 3751e52b2b3242f924c99d9b87ab4134

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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3751e52b2b3242f924c99d9b87ab4134
Registration Details
Taiwan FDA Registration: 3751e52b2b3242f924c99d9b87ab4134
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Device Details

"Telifano" pressure injection type peripherally placed in the central venous catheter group
TW: โ€œๆณฐๅˆฉ็ฆไบž่ซพโ€ ๅฃ“ๅŠ›ๆณจๅฐ„ๅž‹้€ฑ้‚Š็ฝฎๅ…ฅไธญๅคฎ้œ่„ˆๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

3751e52b2b3242f924c99d9b87ab4134

DHA05603430401

Product Details

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

J General hospital and personal use equipment

J.5970 Percutaneous long-term implantable endovascular catheters

import

Dates and Status

Jan 13, 2021

Jan 13, 2026

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