Medical device. Before using the medical products offered on this information resource, it is recommended to consult your doctor and read the instructions. Correspondence certificate UMCC #UA.TR.039.186-16 as of 30.06.2016. Information about medical products for the professional work of health professionals.
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Good manufacturing practices (GMP) are the practices required in order to conform to the guidelines recommended by agencies that control authorization and licensing for manufacture and sale of drug products, and active pharmaceutical products.
Meets NATO standards
As part of the individual medical kits, according to NATO standards, there is a hemostatic dressing, plugged with hemostatic agent. Plugging bandage stops the bleeding neck, trunk and allows enfeeble tourniquet at wound limbs.
Made in Ukraine
We contribute to the development of society through responsible and careful attitude to the quality of our products, the preservation of the environment, and also by supporting social and charitable projects.Learn more.
ISO, the International Organization for Standardization. ISO 13485, Medical devices – Quality management systems – Requirements for regulatory purposes, is an internationally agreed standard that sets out the requirements for a quality management system specific to the medical devices industry.
ISO, the International Organization for Standardization. ISO 9001-2009.This standard is based on a number of quality management principles including a strong customer focus, the motivation and implication of top management, the process approach and continual improvement.