Taiwan FDA registration 09afd4ae4558c77273123cbb90ebfda6

GE blood glucose monitoring systems

TW: GE 血糖監測系統
Taiwan flagTaiwan·Risk Class 2·Daqing Factory of Huaguang Biotechnology Co., Ltd·Registered Nov 25, 2020 – Nov 25, 2025Expired
Registration details
Analysis ID
09afd4ae4558c77273123cbb90ebfda6
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
This product is used as an in vitro diagnostic reagent for users to self-measure the blood glucose value of the fingertip, palm or arm whole blood, or professionals to measure the blood glucose value of microvascular whole blood collected by the fingertip, palm or arm of others, as well as the blood glucose value of vein, artery and neonatal whole blood.
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
Nov 25, 2020
Expiry Date
Nov 25, 2025
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About this record

Access comprehensive regulatory information for GE blood glucose monitoring systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09afd4ae4558c77273123cbb90ebfda6 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 3 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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