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“ARKRAY” Fully Automated Urine Analyzer Aution Max AX-4030(Non-Sterile) - Taiwan Registration a19993b2d667d58d46b5c26a621a0971

Access comprehensive regulatory information for “ARKRAY” Fully Automated Urine Analyzer Aution Max AX-4030(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a19993b2d667d58d46b5c26a621a0971 and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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a19993b2d667d58d46b5c26a621a0971
Registration Details
Taiwan FDA Registration: a19993b2d667d58d46b5c26a621a0971
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Device Details

“ARKRAY” Fully Automated Urine Analyzer Aution Max AX-4030(Non-Sterile)
TW: “愛科來”自動尿液分析儀 AX-4030(未滅菌)
Risk Class 1
MD

Registration Details

a19993b2d667d58d46b5c26a621a0971

Ministry of Health Medical Device Import Registration No. 008772

DHA08400877205

Company Information

Japan

Product Details

Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A2900 Automated Urinalysis System

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025