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“ARKRAY” AUTION CHECK PLUS - Taiwan Registration 4490450e3bf3b07f8d79e0ac664a5bf8

Access comprehensive regulatory information for “ARKRAY” AUTION CHECK PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4490450e3bf3b07f8d79e0ac664a5bf8 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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4490450e3bf3b07f8d79e0ac664a5bf8
Registration Details
Taiwan FDA Registration: 4490450e3bf3b07f8d79e0ac664a5bf8
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Device Details

“ARKRAY” AUTION CHECK PLUS
TW: “愛科來” 第二代尿液品管液
Risk Class 2
MD

Registration Details

4490450e3bf3b07f8d79e0ac664a5bf8

Ministry of Health Medical Device Import No. 035216

DHA05603521606

Company Information

Japan

Product Details

This product is used to detect the quality management of AUTION Sticks and AUTION SCREEN Microalbumin/Creatinine and other urine systems.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad; GMP

Dates and Status

Feb 09, 2022

Feb 09, 2027