Taiwan FDA registration 5966d03ce43fbd8127cd8ddc4e3599f5
“MIKO”IV Monitoring System
TW: “MIKO”點滴監測系統
Taiwan·Risk Class 2·MD·Yongpan Technology Co., Ltd·Registered Nov 23, 2022 – Nov 23, 2027ActiveRegistration details
- Analysis ID
- 5966d03ce43fbd8127cd8ddc4e3599f5
- License Form
- Ministry of Health Medical Device Manufacturing No. 007775
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
- Nov 23, 2022
- Expiry Date
- Nov 23, 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 5966d03ce43fbd8127cd8ddc4e3599f5 and manufactured by Yongpan Technology Co., Ltd. The authorized representative in Taiwan is Yongpan Technology Co., Ltd.
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