Taiwan FDA registration 54a9215389f4775fea6f17ad7a7d6171

Metrojet Unimax Uric Acid Testing System (Unsterilized)

TW: 百捷優邁尿酸檢驗系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Qinli Biotechnology Co., Ltd. New North Plant·Registered Aug 15, 2022 – Aug 15, 2027Active
Registration details
Analysis ID
54a9215389f4775fea6f17ad7a7d6171
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the "uric acid test system (A.1775)" of the Measures for the Classification and Grading Management of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1775 尿酸試驗系統
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Aug 15, 2022
Expiry Date
Aug 15, 2027
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About this record

Access comprehensive regulatory information for Metrojet Unimax Uric Acid Testing System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 54a9215389f4775fea6f17ad7a7d6171 and manufactured by Qinli Biotechnology Co., Ltd. New North Plant. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Qinli Biotechnology Co., Ltd. new tree factory, and 1 recent registrations in the same category. 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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