"ARKRA" urinalysis tester (unsterilized)
Taiwan·Risk Class 1·ARKRAY INDUSTRY, INC.·Registered Jan 06, 2016 – Jan 06, 2026Cancelled- Analysis ID
- be17802aba2a879884a164d04d7044bf
- Customs Code
- DHA09401605100
- Manufacturer
- ARKRAY INDUSTRY, INC.
- Manufacturer Country
- Philippines
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
- 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)
- A.2900 Automated urinalysis system
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Jan 06, 2016
- Expiry Date
- Jan 06, 2026
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "ARKRA" urinalysis tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be17802aba2a879884a164d04d7044bf and manufactured by ARKRAY INDUSTRY, INC.. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Arkray Factory Inc., Head office factory, ARKRAY INDUSTRY, INC., and 2 recent registrations in the same category. 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.