Taiwan FDA registration f23199bce1e13ea72c17deba6ac4b9c7
Beckman Coulter Automated Urine Chemical Analysis System (Unsterilized)
TW: 貝克曼庫爾特 自動尿液化學分析系統 (未滅菌)
Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Aug 30, 2023 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- f23199bce1e13ea72c17deba6ac4b9c7
- Customs Code
- DHA084a0021801
Company information
- Manufacturer
- BECKMAN COULTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of the "Automated Urinalysis System (A.2900)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2900 Automated urinalysis system
Dates and status
- Registration Date
- Aug 30, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Beckman Coulter Automated Urine Chemical Analysis 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 f23199bce1e13ea72c17deba6ac4b9c7 and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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