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 µg/mL) for the quality control of ARIXTRA® (Fondaparinux) testing using anti-Xa colorimetric assays.
Quality control of ARIXTRA® testing (BIOPHEN Heparin).
Specific for ARIXTRA®.ARIXTRA is a registered trademark of GlaxoSmithKline.
Please Note: IVD Not for Sale in US. For US availability CLICK HERE.
Instructions For Use
Material Safety Data Sheet (MSDS)
Certificate of Analysis (COA)