Taiwan FDA registration c095441e52964271baf044fe669fd329
Beckman Coulter stem cells control cells
TW: 貝克曼庫爾特幹細胞控制細胞
Registration details
- Analysis ID
- c095441e52964271baf044fe669fd329
- Customs Code
- DHA00601786601
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 qualitative quality control product at known concentration, which can be used for immunodominant typing analysis and flow cytometry using CD45 and/or CD34 monoclonal antibodies as reagents.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Jan 03, 2007
- Expiry Date
- Jan 03, 2027
About this record
Access comprehensive regulatory information for Beckman Coulter stem cells control cells in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c095441e52964271baf044fe669fd329 and manufactured by IMMUNOTECH SAS, A BECKMAN COULTER COMPANY. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details. 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.
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