Medical Technologies

Reagent Kit for Fibrinogen Determination in Blood Plasma by Clotting Method (Fibrinogen Test) in Accordance with TU 21.20.23-068-05595541-2020

Reagent Kit for Fibrinogen Determination in Blood Plasma by Clotting Method (Fibrinogen Test) in Accordance with TU 21.20.23-068-05595541-2020

The reagent kit is designed for the determination of fibrinogen levels in human blood plasma using the clotting method. Complies with TU 21.20.23-068-05595541-2020.

I. Fibrinogen Test – Available Variants:

Variant 1 (Manufacturer's catalog number: PG-10/1):

  • Thrombin, lyophilized – 8 vials (each vial reconstitutes to 2.0 mL)
  • Plasma calibrator, lyophilized – 1 vial (reconstituted volume: 1.0 mL)
  • Imidazole buffer – 1 vial (5.0 mL)

Variant 2 (Manufacturer's catalog number: PG-10/2):

  • Thrombin, lyophilized – 8 vials (each vial reconstitutes to 5.0 mL)
  • Plasma calibrator, lyophilized – 1 vial (reconstituted volume: 1.0 mL)
  • Imidazole buffer – 1 vial (5.0 mL)

Variant 3 (Manufacturer's catalog number: PG-10/3):

  • Thrombin, liquid – 8 vials (5.0 mL each)
  • Plasma calibrator, lyophilized – 1 vial (reconstituted volume: 1.0 mL)
  • Imidazole buffer – 1 vial (5.0 mL)

II. Instructions for Use

III. Medical Device Passport


If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Fibrinogen Determination in Blood Plasma by Clotting Method (Fibrinogen Test) in Accordance with TU 21.20.23-068-05595541-2020, 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.

Copyright MAXXmarketing GmbH
JoomShopping Download & Support