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“MIKO”IV Monitoring System - Taiwan Registration 5966d03ce43fbd8127cd8ddc4e3599f5

Access comprehensive regulatory information for “MIKO”IV Monitoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5966d03ce43fbd8127cd8ddc4e3599f5 and manufactured by Yongpan Technology Co., Ltd. The authorized representative in Taiwan is Yongpan Technology 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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5966d03ce43fbd8127cd8ddc4e3599f5
Registration Details
Taiwan FDA Registration: 5966d03ce43fbd8127cd8ddc4e3599f5
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Device Details

“MIKO”IV Monitoring System
TW: “MIKO”點滴監測系統
Risk Class 2
MD

Registration Details

5966d03ce43fbd8127cd8ddc4e3599f5

Ministry of Health Medical Device Manufacturing No. 007775

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J2420 Electronic Monitor for Gravimetric Infusion Systems

Produced in Taiwan, China

Dates and Status

Nov 23, 2022

Nov 23, 2027