Taiwan FDA registration 23b315f884ddaad25a7fffa2f51b9ea2

"AGRA" Automatic Urine Analyzer (Unsterilized)

TW: "愛科來" 全自動尿液分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·ARKRAY FACTORY, INC.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
23b315f884ddaad25a7fffa2f51b9ea2
Customs Code
DHA08401610106
Company information
Manufacturer Country
Japan
Authorized Representative
MEDTRI CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Automated Urinalysis System (A.2900)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2900 Automated urinalysis system
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "AGRA" Automatic Urine Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23b315f884ddaad25a7fffa2f51b9ea2 and manufactured by ARKRAY FACTORY, INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARKRAY FACTORY, INC., 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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