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"MIKO" Urine Bag Monitoring System (Non-Sterile) - Taiwan Registration e508e93904b267a72e9a32fb8b930881

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.

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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e508e93904b267a72e9a32fb8b930881
Registration Details
Taiwan FDA Registration: e508e93904b267a72e9a32fb8b930881
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Device Details

"MIKO" Urine Bag Monitoring System (Non-Sterile)
TW: "MIKO" ๅฐฟ่ข‹็›ฃๆธฌ็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e508e93904b267a72e9a32fb8b930881

Company Information

Taiwan, Province of China

Product Details

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.

H Gastroenterology and urology

H.1800 ๅฐฟๆถฒๆต้‡ๆˆ–ๅฎน็ฉๆธฌ้‡็ณป็ตฑ

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Nov 27, 2024

Nov 27, 2029