Disinfectant. The Product Should Be A Colorless Liquid (Ready Solution) With A Characteristic Odor Of Alcohol. The Active Ingredients Should Contain N-Propanol - 52.3-57.7%, Didecyldimethylammonium Chloride - 0.135 - 0.22%. The Product Should Not Contain Isopropyl Or Ethyl Alcohol, Hydrogen Peroxide, Triamine, Guanidine, Fragrances, Or Dyes. Purpose: For Quick Disinfection Of Small-Sized And Hard-To-Reach Indoor Surfaces, Furnishings, Instruments, Medical Equipment, Rugs For Bacterial, Viral And Fungal (Candidiasis, Dermatophytosis) Infections In Medical Organizations Of Any Profile (Including Childrens Departments And Neonatology Departments), For Emergency Disinfection Of Surfaces. The Maximum Permissible Surface Area To Be Treated Should Be No More Than 1/10 Of The Total Area Of The Room. There Is No Need To Rinse The Product From Treated Surfaces After Disinfection. A One-Time Treatment Should Be Carried Out Using Wiping And Irrigation Methods. The Shelf Life Of The Product Is At Least 5 Years. A Bottle Of At Least 750 Ml With A Trigger Spray. Availability Of A Certificate., Disinfectant (Skin Antiseptic) It Is A Ready-To-Use Skin Antiseptic In The Form Of A Clear, Colorless Liquid With The Smell Of Ethyl Alcohol. Antiseptic Composition: Purified Ethyl Alcohol Not Less Than 70%, Polyhexamethylene Guanidine Hydrochloride Not More Than 0.1%, Alkyldimethylbenzylammonium Chloride Not More Than 0.15%, As Well As Skin Softening Components And Functional Additives. The Product Must Have Antimicrobial Activity Against Gram-Positive And Gram-Negative Bacteria, Including Against Pathogens Causing Nosocomial Infections, Including Methicillen-Resistant Staphylococcus, Vancomycin-Resistant Enterococcus, Pseudomonas Aeruginosa, Tuberculocidal, Virucidal, Including Enteral And Parenteral Hepatitis Viruses (Including Hepatitis A, B And C), Hiv, Polio, Adenoviruses, Enteroviruses, Rotaviruses, Coronaviruses (Including Covid-2019), Sars Viruses, Bird Flu H5n1, Swine Flu A/H1n1, Human Influenza, Herpes, Etc.), Action. A Bottle With A Volume Of At Least 1.0 Liters. The Products Shelf Life Is At Least 5 Years From The Date Of Manufacture In Unopened Manufacturers Packaging. Availability Of A Certificate., The Disinfectant Must Be In The Form Of Tablets With A Characteristic Odor Of Chlorine, Weighing At Least 3.33 G, Releasing From 1.35 To 1.65 G Of Active Chlorine When Dissolved In Water. The Jar Contains At Least 1 Kilogram. The Minimum Disinfection Regime For Bacterial And Viral Infections Should Be 0.0075%, The Yield Of The Working Solution From 1 Tablet Should Be At Least 20 Liters. The Composition Must Contain Sodium Salt Of Dichloroisocyanuric Acid (Dihydrate) - 80.5%, As Well As Adipic Acid, Sodium Carbonate And Bicarbonate, Ph Of The Product - No Less Than 5.0 - No More Than 7.0, The Composition Of The Product Must Be Confirmed By Official Documents Issued By Authorized Bodies. The Shelf Life Of The Product Is At Least 7 Years In Unopened Manufacturers Packaging, Working Solutions Are At Least 30 Days. The Product Has Antimicrobial Activity Against Bacteria (Including Mycobacterium Tuberculosis And Bacilli Spores), Viruses, Fungi Of The Genus Candida And Trichophyton And Is Intended For Disinfecting Indoor Surfaces, Hard Furniture, Sanitary Equipment, External Surfaces Of Devices And Apparatus, Medical Products (From Corrosion-Resistant Metals, Rubbers, Plastics, Glass), Linen, Dishes, Including Laboratory Dishes, Items For Washing Dishes, Shoes Made Of Rubber, Plastics And Other Polymeric Materials, Patient Care Items, Cleaning Equipment, Medical Waste, Rubber Mats For Infections Of Bacterial (Including Tuberculosis), Viral And Fungal (Candidiasis And Dermatophytosis) Etiology During Preventive, Current And Final Disinfection In Medical And Preventive Institutions (Hci), Including Obstetric Hospitals (Except For Neonatology Departments), Clinical, Microbiological And Other Laboratories, In Infectious Foci. Availability Of A Certificate., The Disinfectant Should Be In The Form Of Tablets With A Characteristic Odor Of Chlorine, Releasing From 1.35 To 1.65 G Of Active Chlorine When Dissolved In Water, Containing At Least 56% Active Chlorine. The Jar Contains At Least 1 Kilogram. The Composition Must Contain Dihydrate Sodium Salt Of Dichloroisocyanuric Acid From 97.8 To 99.8%. Working Solutions Must Have Increased Wetting Ability, Which Improves The Quality Of Treatment Of Surfaces With Microcracks And Roughness, As Well As Improves Adhesion To Hydrophobic Surfaces Due To The Presence Of N,N-(Biphenyl-4,4-Diyl-Bis(Methylene-Bis(N,N-Dimethyldodecane-1-Aminium) Dichloride - 0.20%), Ph From Not Less 5.0 - No More Than 7.0. Shelf Life Of The Product Is 7 Years In Unopened Manufacturers Packaging, Working Solutions Are At Least 30 Days. Availability Of A Certificate., Disinfectant Soap Should Be A Ready-To-Use Colorless Or Light Yellow Transparent Or Slightly Opalescent Gel-Like Mass. The Product Must Contain 2,4,4-Trichloro-2-Hydroxydiphenyl Ether (Triclosan) As An Active Ingredient - 0.25%, As Well As Functional Additives, Moisturizing And Skin Care Components, Ph Of At Least 10% Of The Aqueous Solution Of The Product - No Less Than 5.0 - No More Than 8.5. The Product Must Have A Bactericidal, Including Tuberculocidal (Mycobacterium Terrae), Fungicidal Effect. The Product Should Not Contain Alcohol, Hac, 2-Phenoxyethanol, Triamine, Glutaraldehyde, Chlorhexidine Bigluconate, Sodium Laureate Sulfate, Acids, Fragrances, Dyes, Sodium Chloride. Purpose: For Washing The Hands Of Surgeons And Operating Medical Personnel Before Treatment With An Antiseptic; Hygienic Treatment Of Hands Before And After Medical Procedures By Workers Of Medical Organizations, Hygienic Treatment Of Hands Of Laboratory Employees; For Sanitary Treatment Of Skin (Hygienic Shower) Of Medical Personnel And Patients In Medical Organizations. Bottle With A Volume Of At Least 1.0 L. Availability Of A Certificate., Disinfectant (Skin Antiseptic) It Is A Ready-To-Use Skin Antiseptic In The Form Of A Clear, Colorless Liquid With The Smell Of Ethyl Alcohol. Antiseptic Composition: Purified Ethyl Alcohol Not Less Than 70%, Polyhexamethylene Guanidine Hydrochloride Not More Than 0.1%, Alkyldimethylbenzylammonium Chloride Not More Than 0.15%, As Well As Skin Softening Components And Functional Additives. The Product Must Have Antimicrobial Activity Against Gram-Positive And Gram-Negative Bacteria, Including Against Pathogens Causing Nosocomial Infections, Including Methicillen-Resistant Staphylococcus, Vancomycin-Resistant Enterococcus, Pseudomonas Aeruginosa, Tuberculocidal, Virucidal, Including Enteral And Parenteral Hepatitis Viruses (Including Hepatitis A, B And C), Hiv, Polio, Adenoviruses, Enteroviruses, Rotaviruses, Coronaviruses (Including Covid-2019), Sars Viruses, Bird Flu H5n1, Swine Flu A/H1n1, Human Influenza, Herpes, Etc.), Action. A Bottle With A Volume Of At Least 5.0 Liters. The Products Shelf Life Is At Least 5 Years From The Date Of Manufacture In Unopened Manufacturers Packaging. Availability Of A Certificate.
