"Beckman Coulter" blood bank centrifuge for in vitro diagnostics (unsterilized)
Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered May 16, 2019 – May 16, 2024Cancelled- Analysis ID
- 03dbf18081887db1552aaf32dae582f1
- Customs Code
- DHA09402045401
- 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 blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- Input;; QMS/QSD
- Registration Date
- May 16, 2019
- Expiry Date
- May 16, 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 "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 03dbf18081887db1552aaf32dae582f1 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, 1 companies making similar products including BECKMAN COULTER, INC., and 5 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.