FVIII:C Deficient Plasma (1 x 1 mL)
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Product DescriptionIn EU: This Product is CE Marked.
Health Canada Licensed. Immunodepleted Factor VIII (FVIII) deficient plasma. <1% residual FVIII activity. Lyophilized human citrated plasma for FVIII clotting activity measurement using one-stage clotting method with CEPHEN. Clinical use: hemophilia A diagnosis and severity classification. Calibrate with BIOPHEN Plasma Calibrator (222101). CE-IVD. 1x1 mL. Product Characteristics
Product Components
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Product ApplicationsFor measurement of Factor VIII:C (FVIII:C) activity. For any in vitro protocol or research study where a source of human FVIII:C deficient plasma is required. Associated calibrator and controls are available: BIOPHEN Plasma Calibrator (Ref A222101-CAN), BIOPHEN Normal Control Plasma (Ref A223201-CAN) and BIOPHEN Abnormal Control Plasma (Ref A223301-CAN). Please Note: IVD Not for Sale in US. For US availability CLICK HERE. Certificate of Analysis (COA) |
FVIII:C Deficient Plasma (1 x 1 mL) - CE / HCL