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"MIKO" IV Monitoring System - Taiwan Registration b5e287052fedd9b4e701e41d4c24789b

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 b5e287052fedd9b4e701e41d4c24789b 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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b5e287052fedd9b4e701e41d4c24789b
Registration Details
Taiwan FDA Registration: b5e287052fedd9b4e701e41d4c24789b
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Device Details

"MIKO" IV Monitoring System
TW: "MIKO" ้ปžๆปด็›ฃๆธฌ็ณธ็ตฑ
Risk Class 2
MD

Registration Details

b5e287052fedd9b4e701e41d4c24789b

Ministry of Health Medical Device Manufacturing No. 007446

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

Mar 11, 2022

Mar 11, 2027