Taiwan FDA registration e2b8a1144e5435d93fdcc27716ad1e92
Beckman Coulter IO detects CD2 monoclonal antibodies
TW: 貝克曼庫爾特IO檢測CD2 單株抗體
Taiwan·Risk Class 2·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Aug 15, 2006 – Aug 15, 2026ActiveRegistration details
- Analysis ID
- e2b8a1144e5435d93fdcc27716ad1e92
- Customs Code
- DHA00601728201
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
- This fluorescently calibrated antibody allows the identification and calculation of cell populations expressing CD2 antigens in human biological samples using flow cytometry.
- 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
- Aug 15, 2006
- Expiry Date
- Aug 15, 2026
About this record
Access comprehensive regulatory information for Beckman Coulter IO detects CD2 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 e2b8a1144e5435d93fdcc27716ad1e92 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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