Taiwan FDA registration 37f126cfe98ef1f8f92ec797673bf9ad
Beckman Coulter IO detects CD3-FITC/CD4-PE monoclonal antibodies
TW: 貝克曼庫爾特 IO檢測CD3-FITC / CD4-PE 單株抗體
Taiwan·Risk Class 2·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Sep 29, 2006 – Sep 29, 2026ActiveRegistration details
- Analysis ID
- 37f126cfe98ef1f8f92ec797673bf9ad
- Customs Code
- DHA00601755201
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 cocktail with flow cytometry for multiplex analysis. It can be used to detect CD3 and CD4 antigens on white blood cells.
- 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-FITC/CD4-PE 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 37f126cfe98ef1f8f92ec797673bf9ad 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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