Taiwan FDA registration a19993b2d667d58d46b5c26a621a0971
“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)
Taiwan·Risk Class 1·MD·ARKRAY FACTORY INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- a19993b2d667d58d46b5c26a621a0971
- License Form
- Ministry of Health Medical Device Import Registration No. 008772
- Customs Code
- DHA08400877205
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, 2025
About this record
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..
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