Request For Quotation Purchasing A Disinfectant

Antiseptic. Disinfectant (Skin Antiseptic) 1L.The Disinfectant Should Be A Ready-To-Use Skin Antiseptic In The Form Of A Clear, Colorless Liquid For Hygienic Use. Treatment Of The Hands Of Medical Staff, Surgeons And Persons Involved In Surgical Interventions, Treatment Of The Elbow Bends Of Donors, Treatment Of The Skin Of The Operating Room And Injection Fields, And Also Have Good Cleaning Properties For Disinfecting Surfaces And Various Objects By Wiping Or Irrigation. The Product Must Contain Ethyl Alcohol Not Less Than 68.0 And Not More Than 77.0%, Chlorhexidine Bigluconate Not Less Than 0.90 And No More Than 1.10%, As Well As Skin Softening Components And Functional Additives. The Product Should Not Contain Acids, Alkalis, Peroxides, Quaternary Ammonium Compounds, Amines, Phenols, Aldehydes, And Their Derivatives, Other Types/Subtypes Of Alcohols. Ph From 5.5 To 7.5. The Product Must Have Antimicrobial Activity Against Gram-Positive And Gram-Negative Bacteria (Including Pathogens Of Nosocomial Infections, Mycobacterium Tuberculosis, Intestinal Infections), Viruses (Acute Respiratory Viral Infections, Herpes, Polio, Hepatitis Of All Types, Including Hepatitis A, B And C, Hiv Infection, Adenovirus, Etc.), Fungi Of The Genus Candida, Trichophyton, And Also Be Active Against The Pathogen M. Terrae. Due To High Alcohol Content The Product Must Have A Prolonged Effect Of At Least 10 Hours (With Confirmation Of A Research/Test Protocol Issued No Earlier Than 2025). Volume 1 Liter With Special. Pump Device. The Product Must Comply With St Rk 3721-2021. Euro Bottles With 1 Liter Pump, (Antibacterial Soap): The Disinfectant In The Form Of Antibacterial Liquid Soap Should Is A Viscous, Homogeneous, Colorless Gel-Like Liquid. Contains As Active Ingredient: Alkyldimethylbenzylammonium Chloride Not Less Than 1.0 But Not More Than 1.2%, Surfactants Not Less Than 5.0 But Not More Than 5.5%, Chlorhexidine Gluconate (Chg) Not Less Than 1.0 But Not More Than 1.2%, Chloroxylenol (Pcmx, Para-Chloro-Meta-Xylenol) Not Less Than 1.0 But Not More Than 1.2%, As Well As Auxiliary Components, Including For Hand Skin Care. The Ph Of The Product Is From 6.0 To 7.0. Density Of The Product At 20ºс, G/Cm³1.02 ± 0.02. The Product Must Have Bactericidal Activity Against Gram-Negative And Gram-Positive Microorganisms, As Well As Fungicidal Activity. The Product Must Be Intended: * For Hygienic Treatment Of The Hands Of Surgeons, Operating Nurses, And Other Persons Involved In Operations, Before Treatment With An Antiseptic; * For Hygienic Treatment Of The Hands Of Medical Personnel In Medical And Preventive Institutions And Organizations (Health Care Facilities And Health Care Facilities) Of Various Profiles (Including Obstetrical And Gynecological, Dental, Oncological, Surgical, Hematological, Infectious Diseases, Dermatovenerological), Pediatric Institutions, Medical And Obstetric Centers, Pathological Institutions, Blood Transfusion Stations And Emergency Medical Care, Sanitary Inspection Stations; * Laboratory Workers; * For Sanitizing The Skin Of Patients (Including Bedridden Patients) Medical And Preventive Institutions And Organizations (Health Care Facilities And Healthcare Facilities) Various Profiles Before Surgical Interventions And During Daily Care In Order To Prevent Bedsores; The Product Must Comply With St Rk Gost R 31696-2017. The Shelf Life Of The Drug Is 1 Year. Canister 5 Liters., Concentrate For Tld Endoscopes. The Disinfectant (Ready Solution) Must Contain Orthophthalic Aldehyde As An Active Substance In The Range Of 0.6-0.65%, As Well As Surfactants, Auxiliary Components And Water. The Product Should Not Contain Other Active Ingredients. The Ph Should Be 7.0-8.5%. The Product Must Have Virucidal, Bactericidal, Tuberculocidal (Against The Pathogen M. Terrae), Fungicidal, Sporicidal Activity. The Product Must Be Well Compatible With Various Materials Of Medical Products, Not Destroy The Surface Being Treated, Not Cause Corrosion Of Metals, Including Aluminum, Carbon Steel, Chromium And Nickel, Not Destroy Adhesive Compounds And Elastomers, And Not Cause Clouding Of Optics. The Product Should Have Reduced Foaming. The Product Must Be Approved For Use For The Disinfection Of Medical Devices Made Of Various Materials, Rigid And Flexible Endoscopes, And Instruments For Them, Manually, Mechanized And Automated; Tld Of Rigid And Flexible Endoscopes In Manual, Mechanized And Automated Ways (Automatic Installation For Washing And Tld Of Endoscopes). The Disinfection Time For Medical Devices At A Product Temperature Of 20 ± 2 Should Be No More Than 5 Minutes, At A Product Temperature Of 25 + 2 °C Should Be No More Than 4 Minutes. Tld Of Endoscopes Manually And Mechanized At A Medium Temperature Of 20 ± 2 °C Should Be No More Than 5 Minutes. Tld Of Endoscopes In An Automated Way At A Medium Temperature Of 25 + 2 ° C Should Be No More Than 4 Minutes. Shelf Life Is At Least 3 Years In Unopened Manufacturers Packaging, In An Opened Canister For At Least 80 Days. Repeated Use Of The Product For At Least 30 Days. For Express Control, Each 4 Canisters Of The Product Must Be Accompanied By 1 Package Of Indicator Strips For Determining Iec Dv. The Minimum Effective Concentration (Mec) Of The Product Must Be Confirmed By A Test Report From An Accredited Laboratory. Canister With A Volume Of At Least 5 Liters., Antiseptic. Disinfectant (Skin Antiseptic) 100Ml. The Disinfectant Must Be A Ready-To-Use Skin Antiseptic In The Form Of A Clear, Colorless Liquid For Hygienic Use. Treatment Of The Hands Of Medical Staff, Surgeons And Persons Involved In Surgical Interventions, Treatment Of The Elbow Bends Of Donors, Treatment Of The Skin Of The Operating Room And Injection Fields, And Also Have Good Cleaning Properties For Disinfecting Surfaces And Various Objects By Wiping Or Irrigation. The Product Must Contain Ethyl Alcohol Not Less Than 68.0 And Not More Than 77.0%, Chlorhexidine Bigluconate Not Less Than 0.90 And No More Than 1.10%, As Well As Skin Softening Components And Functional Additives. The Product Should Not Contain Acids, Alkalis, Peroxides, Quaternary Ammonium Compounds, Amines, Phenols, Aldehydes, And Their Derivatives, Other Types/Subtypes Of Alcohols. Ph From 5.5 To 7.5. The Product Must Have Antimicrobial Activity Against Gram-Positive And Gram-Negative Bacteria (Including Pathogens Of Nosocomial Infections, Mycobacterium Tuberculosis, Intestinal Infections), Viruses (Acute Respiratory Viral Infections, Herpes, Polio, Hepatitis Of All Types, Including Hepatitis A, B And C, Hiv Infection, Adenovirus, Etc.), Fungi Of The Genus Candida, Trichophyton, And Also Be Active Against The Pathogen M. Terrae. Due To High Alcohol Content The Product Must Have A Prolonged Effect Of At Least 10 Hours (With Confirmation Of A Research/Test Protocol Issued No Earlier Than 2025). Volume 100 Ml Bottle With Spray. The Product Must Comply With St Rk 3721-2021.