Taiwan FDA registration 33ff1da4c513c72632d07f5e28fc31c3

GE GlucoCapture 血糖監測系統

Taiwan flagTaiwan·Risk Class 2·Daqing Factory of Huaguang Biotechnology Co., Ltd·Registered Mar 17, 2021 – Jul 17, 2028Active
Registration details
Analysis ID
33ff1da4c513c72632d07f5e28fc31c3
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
This product is for in vitro diagnostic use, intended for general personnel (self-test and professional use), to measure fresh whole blood glucose obtained through fingertips, palms or microvessels of the arm, not suitable for newborns.
Product Type (Level 1)
A Clinical Chemistry and Clinical Toxicology;; I General, Plastic Surgery and Dermatology
Product Type (Level 2)
A.1660 Quality control materials (analytical and non-analytical); I.4800 Surgical Hand Instruments for General Surgery;; A.1345 Glucose test system
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Mar 17, 2021
Expiry Date
Jul 17, 2028
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About this record

Access comprehensive regulatory information for GE GlucoCapture 血糖監測系統 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 33ff1da4c513c72632d07f5e28fc31c3 and manufactured by Daqing Factory of Huaguang Biotechnology Co., Ltd. The authorized representative in Taiwan is Daqing Factory of Huaguang Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Daqing Factory of Huaguang Biotechnology Co., Ltd, and 2 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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