"Beckman Coulter" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Oct 01, 2021 – Oct 31, 2024Expired- Analysis ID
- c7f4dfbf143146d3fc8d251de8741717
- Customs Code
- DHA08402045402
- Manufacturer
- BECKMAN COULTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
- Intended Use
- Limited to the classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
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Access comprehensive regulatory information for "Beckman Coulter" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c7f4dfbf143146d3fc8d251de8741717 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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