Taiwan FDA registration 5b37b97c87cde8562e0433907e9defbf

"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 Jan 21, 2016 – Jan 21, 2026Cancelled
Registration details
Analysis ID
5b37b97c87cde8562e0433907e9defbf
Customs Code
DHA09401610102
Company information
Manufacturer Country
Japan
Authorized Representative
MEDTRI CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration 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
Jan 21, 2016
Expiry Date
Jan 21, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 5b37b97c87cde8562e0433907e9defbf 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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