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“Imaxeon” MEDRAD Centargo Patient Line - Taiwan Registration 4857a1e0dfc76e02eefb0d9066be3cee

Access comprehensive regulatory information for “Imaxeon” MEDRAD Centargo Patient Line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4857a1e0dfc76e02eefb0d9066be3cee and manufactured by IMAXEON PTY LTD.. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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4857a1e0dfc76e02eefb0d9066be3cee
Registration Details
Taiwan FDA Registration: 4857a1e0dfc76e02eefb0d9066be3cee
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Device Details

“Imaxeon” MEDRAD Centargo Patient Line
TW: “益邁森” 輸液管套組
Risk Class 2
MD

Registration Details

4857a1e0dfc76e02eefb0d9066be3cee

Ministry of Health Medical Device Import No. 034479

DHA05603447907

Company Information

Australia

Product Details

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

E Cardiovascular devices

E1650 Vascular photography syringes and syringes

Imported from abroad

Dates and Status

Mar 30, 2021

Mar 30, 2026