Control material for quantitative determination of D-dimers content in human blood plasma (ReDimer-control) according to TU 21.2

Designed for use as a control material to assess the correctness and reproducibility of the quantitative determination of D-dimers in human blood plasma. The determination of D-dimers has a high diagnostic significance. The most common use of D-dimer determination for diagnostic purposes is to exclude venous thromboembolic conditions (VTE) - deep vein thrombosis (DVT) and pulmonary embolism (PTE). ReDimer-control is analysed in one series of measurements with the plasma under study when performing quantitative tests of D-Dimer determination according to the instructions attached to the corresponding reagent kits. The analysed parameters of the control material should fall within the range of values specified in the kit data sheet. Kit composition:ReDimer-control level 1, lyophilically dried (volume after reconstitution 1.0 ml/fl.) - 3 vials;ReDimer-control level 2, lyophilically dried (volume after reconstitution 1.0 ml/fl.) - 3 vials.