Taiwan FDA registration b5e287052fedd9b4e701e41d4c24789b
"MIKO" IV Monitoring System
TW: "MIKO" 點滴監測糸統
Taiwan·Risk Class 2·MD·Yongpan Technology Co., Ltd·Registered Mar 11, 2022 – Mar 11, 2027ActiveRegistration details
- Analysis ID
- b5e287052fedd9b4e701e41d4c24789b
- License Form
- Ministry of Health Medical Device Manufacturing No. 007446
Company information
- Manufacturer
- Yongpan Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Yongpan Technology Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J2420 Electronic Monitor for Gravimetric Infusion Systems
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 11, 2022
- Expiry Date
- Mar 11, 2027
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices