Pure Global

“Iradimed” MRidium MRI Infusion Pump and Pulse Oximeter System - Taiwan Registration 5f9c479a3bc7e572e08da2ed34c7d212

Access comprehensive regulatory information for “Iradimed” MRidium MRI Infusion Pump and Pulse Oximeter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5f9c479a3bc7e572e08da2ed34c7d212 and manufactured by Iradimed Corporation. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
5f9c479a3bc7e572e08da2ed34c7d212
Registration Details
Taiwan FDA Registration: 5f9c479a3bc7e572e08da2ed34c7d212
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Iradimed” MRidium MRI Infusion Pump and Pulse Oximeter System
TW: “艾樂得” 輸液系統
Risk Class 2
MD

Registration Details

5f9c479a3bc7e572e08da2ed34c7d212

Ministry of Health Medical Device Import No. 035550

DHA05603555005

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J5725 Infusion pump

Imported from abroad

Dates and Status

Aug 08, 2022

Aug 08, 2027