Taiwan FDA registration 3cb79a139214a6d008d4439a905d5ea2
“ARKRAY” Urine Analysis System Aution Eleven AE-4020(Non-Sterile)
TW: “愛科來”自動尿液分析儀 AE-4020(未滅菌)
Taiwan·Risk Class 1·MD·ARKRAY FACTORY INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 3cb79a139214a6d008d4439a905d5ea2
- License Form
- Ministry of Health Medical Device Import Registration No. 008773
- Customs Code
- DHA08400877307
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” Urine Analysis System Aution Eleven AE-4020(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 3cb79a139214a6d008d4439a905d5ea2 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.
Free DatabasePowered by Pure Global AI89,000+ Devices