Taiwan FDA registration e508e93904b267a72e9a32fb8b930881

"MIKO" Urine Bag Monitoring System (Non-Sterile)

TW: "MIKO" 尿袋監測系統 (未滅菌)

Taiwan·Risk Class 1·Yongpan Technology Co., Ltd·Registered Nov 27, 2024 – Nov 27, 2029Active

Registration details

Analysis ID: e508e93904b267a72e9a32fb8b930881

Company information

Manufacturer: Yongpan Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Yongpan Technology Co., Ltd

Product details

Intended Use: It is limited to the first level of identification of the "Urine Flow or Volume Measurement System (H.1800)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1800 尿液流量或容積測量系統
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Nov 27, 2024
Expiry Date: Nov 27, 2029

About this record

Access comprehensive regulatory information for "MIKO" Urine Bag Monitoring System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e508e93904b267a72e9a32fb8b930881 and manufactured by Yongpan Technology Co., Ltd. The authorized representative in Taiwan is Yongpan Technology Co., Ltd.

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