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The Disinfectant (Concentrate) Must Contain Polyhexamethylene Guanidine Hydrochloride (Phmg) No More Than 2.0%, Benzalkonium Chloride No More Than 4.5% (Qac), As Well As A Surfactant, Complexing Agent And Water. The Product Should Not Contain Aldehydes, Chlorine, Peroxide, Or Acids. Ph Should Be 7.5-10.5. The Product Must Have Bactericidal, Tuberculocidal (Against The Pathogen M. Terrae), Virucidal, Fungicidal Antimicrobial Activity. The Product Must Be Approved For Use For: Disinfection And Cleaning Of Indoor Surfaces; Disinfection (Combined And Not Combined With Pso) Of Medical Devices And Medical Equipment; Disinfection Combined With Pso Of Flexible And Rigid Endoscopes. Shelf Life Is At Least 5 Years, Working Solutions Are At Least 15 Days. The Product Must Be Accompanied By Indicator Strips For Iec Express Control (Up To 100 Liters Of Concentrate 1 Package, Then For Every 100 Liters Of Concentrate 1 Package). A Canister With A Volume Of At Least 5 Liters., A Single-Use Disinfectant (Hereinafter Referred To As The Product) Must Be A Two-Component System Consisting Of Component A And Component B, Mixed When Used In Automatic Reprocessors. Component A Should Be A Colorless Transparent Liquid With A Characteristic Odor Of The Components Used, Containing Hydrogen Peroxide In The Range Of 30.0 ± 5.0%, Peracetic Acid (Paa) In The Range Of 5.0 ± 1.5%, And Ph In The Range Of 3.0 ± 0.5%. Component B Should Be A Transparent Or Light Yellow Liquid With The Smell Of The Components Used, Containing Sodium Tetraborate, Corrosion Inhibitors, Stabilizers, Ph Regulators, Purified Water; Ph In The Range Of 11.5 ± 2.5%. After Mixing Components A And B, The Product Must Contain Peracetic Acid (Paa) In The Range Of 0.12 ± 0.05%, Hydrogen Peroxide In The Range Of 0.7 ± 0.15%, Functional Additives, And Water As Active Ingredients. The Product Must Have Bactericidal, Tuberculocidal, Sterilizing (Sporicidal), Virucidal, Fungicidal Activity, Not Fix Organic Contaminants, And Can Be Easily Washed Off (1 Wash). The Product Must Be Compatible With Medical Devices And Medical Equipment Materials, Including Rigid And Flexible Endoscopes And Automatic Systems For Processing Endoscopes (Reprocessors), Which Use Stainless Steel, Ceramics, Glass, Plastics And Elastomers. The Product Must Be Designed For At Least 52 Endoscope Processing Cycles. The Shelf Life Of Components A And B In Unopened Packaging Must Be At Least 18 Months. The Product Must Be Packaged In Canisters With A Volume Of At Least 10 Liters., A Disinfectant With A Detergent Effect Should Be In The Form Of Tablets With A Separating Line Weighing 3.1 ± 0.4 G. As Active Ingredients, The Composition Should Contain 99.1 ± 0.7% Sodium Salt Of Dichloroisocyanuric Acid And 0.4 ± 0.15% Sodium Dodecyl Sulfate. The Product Should Not Require The Addition Of Additional Detergents. The Content Of Active Chlorine In The Product Should Be 55 ± 3.0%. When 1 Tablet Is Dissolved In Water, 1.5 ± 0.16 G Of Active Chlorine Should Be Released. The Ph Of The Product Should Be In The Range Of 5.5-7.0. The Product Must Have Bactericidal Activity (Including Against Mrsa, Vre, Clostridium), Tuberculocidal Activity (M. Terrae), Fungicidal Activity (Including Against Aspergillus), Virucidal Activity (Including Against Polio Virus And Adenovirus Type 5), Active Against Particularly Dangerous Infections (Plague, Cholera, Tularemia, Brucellosis, Anthrax). The Product Must Be Approved For: - Disinfection Of Indoor Surfaces, Hard Furniture, Sanitary Equipment, External Surfaces Of Devices, Medical Products, For Infections Of Bacterial (Including Tuberculosis), Viral And Fungal Etiology During Preventive, Current And Final Disinfection In Medical Facilities; - Carrying Out General Cleaning. The Shelf Life Of The Product Must Be At Least 7 Years, Working Solutions - 25 Days. The Product Must Contain At Least 1 Kg In One Jar. The Product Must Be Accompanied By Indicator Strips For Iec Express Control (Up To 100 Liters Of Concentrate 1 Package, Then For Every 100 Liters Of Concentrate 1 Package).
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