Hyphen BioMed
BIOPHENâ„¢ Dabigatran Control Low
In EU: This product is CE Marked. Health Canada Licensed. Lyophilized plasmas, at defined Dabigatran concentrations (2 levels of about 15-35 and 45-105 ng/mL), as measured with the HEMOCLOT Thrombin Inhibitors kit, for the quality control of Dabigatran measurements with clotting or chromogenic assays.
BIOPHENâ„¢ FVIIa Control Set
In US: For Research Use Only. Not for Use in Diagnostic Procedures. BIOPHEN FVIIa Control Set kit is a set of controls intended for the quality control of activated Factor VII (FVIIa) activity measurements, using a clotting assay with the HEMOCLOT Factor VIIa kit. This kit is for research use only and must not be used for patient diagnosis or treatment. This is an ON-DEMAND item which requires minimum order quantity and extended lead time. Please Contact Us for a quote.
BIOPHENâ„¢ FXIa Control Set
For Research Use Only. Not for Use in Diagnostic Procedures. BIOPHEN FXIa Control Set is a set of controls intended for the quality control of activated Factor XI (FXIa) activity measurements, using BIOPHEN FXIa colorimetric assay. This kit is optimized using BIOPHEN FXIa assay.
BIOPHENâ„¢ Dabigatran Control Plasma
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Lyophilized plasmas, at defined Dabigatran concentrations (2 levels of about 100 and 300 ng/mL), as measured with the HEMOCLOT Thrombin Inhibitors kit , for the quality control of Dabigatran measurements with clotting or chromogenic assays.
BIOPHENâ„¢ Dabigatran Control Plasma
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. Lyophilized plasmas, at defined Dabigatran concentrations (2 levels of about 100 and 300 ng/mL), as measured with the HEMOCLOT Thrombin Inhibitors kit, for the quality control of Dabigatran measurements with clotting or chromogenic assays.
BIOPHENâ„¢ FIXa Control Set
For Research Use Only. Not for Use in Diagnostic Procedures. Factor IXa Controls are intended for the quality control of activated Factor IX (FIXa) chromogenic measurements, using BIOPHEN Factor IXa assay. This is an ON-DEMAND item which requires minimum order quantity and extended lead time. Please Contact Us for a quote.
BIOPHENâ„¢ Rivaroxaban Control Plasma
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Lyophilized plasmas, at defined Rivaroxaban concentrations (2 levels of about 100 and 300 ng/mL), as measured with the BIOPHEN DiXal, for the quality control of Rivaroxaban measurements using chromogenic assays.
BIOPHENâ„¢ Rivaroxaban Control Plasma
In EU: This Product is CE Marked. Health Canada Licensed. Lyophilized plasmas, at defined Rivaroxaban concentrations (2 levels of about 100 and 300 ng/mL), as measured with the BIOPHEN DiXal, for the quality control of Rivaroxaban measurements using chromogenic assays.
BIOPHENâ„¢ LMWH Control Low Cll
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasma at about 0.50 IU/mL (CII) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the low concentration range.
BIOPHENâ„¢ LMWH Control Low Cll
In US: This product is 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 0.50 IU/mL (CII) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the low concentration range.
BIOPHENâ„¢ LMWH Control Low Cl
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasma at about 0.25 IU/mL (CI) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the low concentration range.
BIOPHENâ„¢ LMWH Control Low Cl
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 0.25 IU/mL (CI) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the low concentration range.
BIOPHENâ„¢ LMWH Control C4
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasma at about 1.20 IU/mL (C4) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the high concentration range.
BIOPHENâ„¢ LMWH Control C4
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 1.20 IU/mL (C4) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the high concentration range.
BIOPHENâ„¢ UFH Control C1
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasma at about 0.20 IU/mL (C1) for the quality control of UFH testing (Unfractionated Heparin).
BIOPHENâ„¢ UFH Control C1
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 0.20 IU/mL (C1) for the quality control of UFH testing (Unfractionated Heparin).
BIOPHEN™ Arixtra® Control Plasma
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Quality control plasmas (2 different levels at about 0.40 and 1.20 g/mL) for the quality control of Arixtra (Fondaparinux) testing using anti-Xa colorimetric assays.
BIOPHEN™ Arixtra® Control Plasma
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasmas (2 different levels at about 0.40 and 1.20 g/mL) for the quality control of Arixtra (Fondaparinux) testing using anti-Xa colorimetric assays.
BIOPHENâ„¢ UFH Control C2
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasma at about 0.50 IU/mL (C2) for the quality control of UFH testing (Unfractionated Heparin).
BIOPHENâ„¢ UFH Control C2
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 0.50 IU/mL (C2) for the quality control of UFH testing (Unfractionated Heparin).
BIOPHENâ„¢ UFH Control C2
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 0.50 IU/mL (C2) for the quality control of UFH testing (Unfractionated Heparin).
BIOPHENâ„¢ LMWH Control C3
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasma at about 0.80 IU/mL (C3) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the high concentration range.
BIOPHENâ„¢ LMWH Control C3
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma at about 0.80 IU/mL (C3) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the high concentration range.
BIOPHENâ„¢ LMWH Control Low
In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasmas (2 different levels: about 0.25 and 0.50 IU/mL) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the low concentration range.
BIOPHENâ„¢ LMWH Control Low
In US: 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasmas (2 different levels: about 0.25 and 0.50 IU/mL) for the quality control of LMWH testing (Low Molecular Weight Heparin), in the low concentration range.
BIOPHENâ„¢ Normalplasma 5
In US and Canada: For Research Use Only. Not for Use in Diagnostic Procedures. Non-titrated normal citrated human plasma, lyophilized. This plasma is useful at any time when a source of normal citrated human plasma is required. Coagulation factors and clotting assays are within the normal range.
BIOPHENâ„¢ Normalplasma 2
In US and Canada: For Research Use Only. Not for Use in Diagnostic Procedures. Non-titrated normal citrated human plasma, lyophilized. This plasma is useful at any time when a source of normal citrated human plasma is required. Coagulation factors and clotting assays are within the normal range.
BIOPHEN™ Orgaran® Control
In US: For Research Use Only. Not for Use in Diagnostic Procedures. Quality control plasmas (2 different levels at about 0.50 and 1.00 U/mL) for the quality control of Sodium Danaparoid testing.
BIOPHEN™ Orgaran® Control
For In Vitro Diagnostic Use. In EU: This Product is CE Marked. Health Canada Licensed. Quality control plasmas (2 different levels at about 0.50 and 1.00 U/mL) for the quality control of Sodium Danaparoid testing.
BIOPHENâ„¢ V-L Control Plasma
In US: This product is 510(k) Cleared for In Vitro Diagnostic Use. Quality control plasma presenting an Activated Protein C Resistance (heterozygous), tested for Factor V-L concentration.
