Taiwan FDA registration 0631b5477a124e2153765d05b268eedd

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 Apr 06, 2021 – Aug 03, 2028Active
Registration details
Analysis ID
0631b5477a124e2153765d05b268eedd
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
This product is specially designed for in vitro diagnostics, which can be used by users to self-measure the blood glucose value of microvascular whole blood collected from fingertips, palms or forearms, or professionals to measure the blood glucose values of microvascular whole blood and vein, arterial and neonatal whole blood collected from other people's fingertips, palms or forearms.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1345 Glucose Test System
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Apr 06, 2021
Expiry Date
Aug 03, 2028
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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 0631b5477a124e2153765d05b268eedd 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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