Ekenvirasti Urinalysis System (Unsterilized)
Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Aug 20, 2019 – Aug 20, 2024Cancelled- Analysis ID
- a2ffeefa60d155035eb9d3af496de719
- Customs Code
- DHA09402078001
- Manufacturer
- BECKMAN COULTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
- 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
- Aug 20, 2019
- Expiry Date
- Aug 20, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for Ekenvirasti Urinalysis System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2ffeefa60d155035eb9d3af496de719 and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including IRIS DIAGNOSTICS, A DIVISION OF IRIS INTERNATIONAL, INC., BECKMAN COULTER, INC., and 4 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.