Medical Technologies

Reagent Kit for Determining the Concentration of Low-Density Lipoprotein Cholesterol (LDL-C) in Serum by Direct Method (LDL-Cholesterol-Novo-A) According to TU 9398-505-23548172-2014

Reagent Kit for Determining the Concentration of Low-Density Lipoprotein Cholesterol (LDL-C) in Serum by Direct Method (LDL-Cholesterol-Novo-A) According to TU 9398-505-23548172-2014

The reagent kit is intended for the quantitative determination of LDL cholesterol in serum using the direct method (LDL-Cholesterol-Novo-A), in compliance with TU 9398-505-23548172-2014.

Available Variants:

  • Variant 1
    Contents:
    • Reagent 1, ready-to-use – 3 vials (20 ml each)
    • Reagent 2, ready-to-use – 1 vial (20 ml)
    • Calibrator based on human serum with LDL cholesterol concentration of 2.38 mmol/L, certified against the reference material NIST SRM1951c
    • The exact concentration of LDL cholesterol in the calibrator may slightly differ from the stated value; the precise concentration is indicated on the vial label and in the certificate
    • Lyophilized – 1 vial
  • Variant 2
    Contents:
    • Reagent 1, ready-to-use – 4 vials (45 ml each)
    • Reagent 2, ready-to-use – 4 vials (15 ml each)

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Determining the Concentration of Low-Density Lipoprotein Cholesterol (LDL-C) in Serum by Direct Method (LDL-Cholesterol-Novo-A) According to TU 9398-505-23548172-2014, then our information portal MEDCOMMERCE can help you with this. To do this, simply fill out the feedback form by clicking on the link FEEDBACK FORM.

The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.

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