Taiwan FDA registration 427892bddf7e1c9851911a6edaa2b500
Beckman Coulter IO detects CD3 monoclonal antibodies
TW: 貝克曼庫爾特IO檢測CD3 單株抗體
Taiwan·Risk Class 2·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Sep 29, 2006 – Sep 29, 2026ActiveRegistration details
- Analysis ID
- 427892bddf7e1c9851911a6edaa2b500
- Customs Code
- DHA00601755102
Company information
- Manufacturer
- IMMUNOTECH SAS, A BECKMAN COULTER COMPANY
- Manufacturer Country
- France
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- A fluorescently calibrated antibody that uses flow cytometry to identify and calculate the population of cells expressing CD3 antigen in human biological samples.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5220 Automatic Differentiation Cell Counter
- Import Information
- import
Dates and status
- Registration Date
- Sep 29, 2006
- Expiry Date
- Sep 29, 2026
About this record
Access comprehensive regulatory information for Beckman Coulter IO detects CD3 monoclonal antibodies in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 427892bddf7e1c9851911a6edaa2b500 and manufactured by IMMUNOTECH SAS, A BECKMAN COULTER COMPANY. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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