Taiwan FDA registration 418d529eea418dae9d797d2993577ad8

"ARKRAY" Automated Urine Analyzer Aution Jet (Non-sterilize)

TW: "愛科來"自動尿液分析儀 (未滅菌)

Taiwan·Risk Class 1·MD·ARKRAY FACTORY INC.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 418d529eea418dae9d797d2993577ad8
License Form: Ministry of Health Medical Device Import Registration No. 009995
Customs Code: DHA08400999504

Company information

Manufacturer: ARKRAY FACTORY INC.
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): A2900 Automated Urinalysis System
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

Access comprehensive regulatory information for "ARKRAY" Automated Urine Analyzer Aution Jet (Non-sterilize) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 418d529eea418dae9d797d2993577ad8 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.